01 2Aspen Pharmacare Holdings
02 12Dr. Reddy's Laboratories
03 9Rusan Pharma
04 4Alkalon AS
05 3Alphapharm PTY Ltd
06 4Apofri AB
07 4Aurobindo Pharma Limited
08 4Aveva Drug Delivery Sytems, Inc
09 3Chattem Chemicals, Inc
10 3DIFGEN PHARMS
11 1Fertin Pharma AS
12 19GSK
13 11Haleon
14 2IVAX Pharmaceuticals Inc
15 14Johnson & Johnson
16 1Magle AB
17 23McNeil Consumer Health
18 7Niconovum AB,
19 1Novartis South Africa (Pty) Ltd
20 4ORIFARM GROUP AS
21 5Omega Pharma AB
22 4Orion Laboratories Pty. Ltd.
23 30PL Developments
24 2PLD ACQUISITIONS
25 4PPI-DAC
26 20Perrigo Company plc
27 2Pfizer Inc
28 4Pharmaceutical Contractors
29 4Pierre Fabre
30 4Samyang Biopharmaceuticals
01 2CAP
02 28CHEWING
03 3CHG
04 7COMPRESSED LOZENGES
05 12FILM, EXTENDED RELEASE;TRANSDERMAL
06 5Film, Extended Release; Transdermal
07 41GUM, CHEWING;BUCCAL
08 1Gum
09 1INH
10 1INHALANT;ORAL
11 1INHALATION VAPOR, LIQUID
12 10LOZENGE
13 3MUNHÅLEPULVER IN SACHET
14 1ORODISPERSIBLE FILM
15 1OROMUCOSAL
16 1OROMUCOSAL SOLUTION
17 9PTD
18 3Patch
19 1SLT
20 3SPO
21 1SPRAY, METERED;NASAL
22 2SUBLINGUAL TABLET
23 3TAB
24 12TRANSDERMAL PATCH
25 40TROCHE/LOZENGE;ORAL
26 9Transdermal Patch
27 9Blank
01 13DISCN
02 1Generic
03 79OTC
04 21Originator
05 1RX
06 95Blank
01 2Complenatal FF
02 2Fruit Nicovel
03 2Fruit Nikorono
04 6HABITROL
05 2Menoflush
06 3NICODERM CQ
07 8NICORETTE
08 2NICORETTE (MINT)
09 1NICORETTE Transdermal Patch 10mg
10 1NICORETTE Transdermal Patch 15mg
11 1NICORETTE Transdermal Patch 25mg
12 1NICORETTE* Quickmist Spray
13 4NICOSTOP
14 3NICOTINE
15 69NICOTINE POLACRILEX
16 3NICOTROL
17 7NiQuitin
18 2NiQuitin Cherries
19 1NiQuitin Citrus
20 3NiQuitin Clear
21 2NiQuitin Mentolmint
22 5NiQuitin Mint
23 1Nicabate P
24 1Nicachet
25 2Nico Pass Liquorice Mint
26 2Nico Pass Mint
27 10Nicorette
28 1Nicorette 2Mg
29 2Nicorette Fruit Mint
30 1Nicorette Inhaler
31 2Nicorette Mentolmint
32 2Nicorette Microtab
33 1Nicorette Microtab Lemon
34 2Nicorette Mint
35 1Nicorette Mint 2Mg
36 3Nicorette Novum
37 5Nicorette Peppermint
38 1Nicorette inhaler
39 2Nicotine Fruit Apofri
40 2Nicotine Mint Apofri
41 2Nicotinell Step 1
42 1Nicotinell Step 2
43 1Nicotinell Step 3
44 1Nicotinell TTS 10
45 1Nicotinell TTS 20
46 1Nicotinell TTS 30
47 2Nicovel Mint
48 2Nikorono Mint
49 4PROSTEP
50 1Quit
51 1Quit 1/2/3/4
52 3QuitX
53 2THRIVE
54 6Zonnic Mint
55 1Zonnic Peppermint
56 1nicorette 16hr Invisipatch
57 9Blank
01 9Australia
02 9India
03 22South Africa
04 4South Korea
05 66Sweden
06 100USA
Regulatory Info : Originator
Registration Country : South Africa
Brand Name : Quit
Dosage Form : SPO
Dosage Strength : 2mg
Packaging : 20X4mg
Approval Date :
Application Number :
Regulatory Info : Originator
Registration Country : South Africa
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info :
Registration Country : USA
Brand Name : HABITROL
Dosage Form : Film, Extended Release; Transdermal
Dosage Strength : 7MG/24HR
Packaging :
Approval Date :
Application Number : 20076
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Transdermal Patch
Dosage Strength : 7mcg/24hr
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Quit 1/2/3/4
Dosage Form : SPO
Dosage Strength : 2mg
Packaging : 80X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info :
Registration Country : USA
Brand Name : HABITROL
Dosage Form : Film, Extended Release; Transdermal
Dosage Strength : 14MG/24HR
Packaging :
Approval Date :
Application Number : 20076
Regulatory Info :
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info :
Registration Country : USA
Brand Name : HABITROL
Dosage Form : Film, Extended Release; Transdermal
Dosage Strength : 21MG/24HR
Packaging :
Approval Date :
Application Number : 20076
Regulatory Info :
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : OTC
Registration Country : USA
Brand Name : HABITROL
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 7MG/24HR
Packaging :
Approval Date : 1999-11-12
Application Number : 20076
Regulatory Info : OTC
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : OTC
Registration Country : USA
Brand Name : HABITROL
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 14MG/24HR
Packaging :
Approval Date : 1999-11-12
Application Number : 20076
Regulatory Info : OTC
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : OTC
Registration Country : USA
Brand Name : HABITROL
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 21MG/24HR
Packaging :
Approval Date : 1999-11-12
Application Number : 20076
Regulatory Info : OTC
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : OTC
Registration Country : USA
Brand Name : NICOTINE POLACRILEX
Dosage Form : TROCHE/LOZENGE;ORAL
Dosage Strength : EQ 2MG BASE
Packaging :
Approval Date : 2020-01-08
Application Number : 212796
Regulatory Info : OTC
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : OTC
Registration Country : USA
Brand Name : NICOTINE POLACRILEX
Dosage Form : TROCHE/LOZENGE;ORAL
Dosage Strength : EQ 4MG BASE
Packaging :
Approval Date : 2020-01-08
Application Number : 212796
Regulatory Info : OTC
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : OTC
Registration Country : USA
Brand Name : NICOTINE POLACRILEX
Dosage Form : TROCHE/LOZENGE;ORAL
Dosage Strength : EQ 2MG BASE
Packaging :
Approval Date : 2020-02-21
Application Number : 212983
Regulatory Info : OTC
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : OTC
Registration Country : USA
Brand Name : NICOTINE POLACRILEX
Dosage Form : TROCHE/LOZENGE;ORAL
Dosage Strength : EQ 4MG BASE
Packaging :
Approval Date : 2020-02-21
Application Number : 212983
Regulatory Info : OTC
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : OTC
Registration Country : USA
Brand Name : NICOTINE POLACRILEX
Dosage Form : TROCHE/LOZENGE;ORAL
Dosage Strength : EQ 2MG BASE
Packaging :
Approval Date : 2020-08-04
Application Number : 213233
Regulatory Info : OTC
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : OTC
Registration Country : USA
Brand Name : NICOTINE POLACRILEX
Dosage Form : TROCHE/LOZENGE;ORAL
Dosage Strength : EQ 4MG BASE
Packaging :
Approval Date : 2020-08-04
Application Number : 213233
Regulatory Info : OTC
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Transdermal Patch
Dosage Strength : 14mcg/24hr
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Transdermal Patch
Dosage Strength : 21mcg/24hr
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Transdermal Patch
Dosage Strength : 7mcg/24hr
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Transdermal Patch
Dosage Strength : 14mcg/24hr
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Transdermal Patch
Dosage Strength : 21mcg/24hr
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Transdermal Patch
Dosage Strength : 7mcg/24hr
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Transdermal Patch
Dosage Strength : 14mcg/24hr
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Transdermal Patch
Dosage Strength : 21mcg/24hr
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : USA
Brand Name : PROSTEP
Dosage Form : Film, Extended Release; Transdermal
Dosage Strength : 11MG/24HR
Packaging :
Approval Date :
Application Number : 19983
Regulatory Info :
Registration Country : USA
Regulatory Info :
Registration Country : USA
Brand Name : PROSTEP
Dosage Form : Film, Extended Release; Transdermal
Dosage Strength : 22MG/24HR
Packaging :
Approval Date :
Application Number : 19983
Regulatory Info :
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROSTEP
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 11MG/24HR
Packaging :
Approval Date : 1998-12-23
Application Number : 19983
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : PROSTEP
Dosage Form : FILM, EXTENDED RELEASE;TRANSDERMAL
Dosage Strength : 22MG/24HR
Packaging :
Approval Date : 1998-12-23
Application Number : 19983
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : NICORETTE
Dosage Form : GUM, CHEWING;BUCCAL
Dosage Strength : EQ 2MG BASE
Packaging :
Approval Date : 1996-02-09
Application Number : 18612
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : NICORETTE (MINT)
Dosage Form : GUM, CHEWING;BUCCAL
Dosage Strength : EQ 2MG BASE
Packaging :
Approval Date : 1998-12-23
Application Number : 18612
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : NICORETTE
Dosage Form : GUM, CHEWING;BUCCAL
Dosage Strength : EQ 2MG BASE
Packaging :
Approval Date : 2000-09-25
Application Number : 18612
Regulatory Info : OTC
Registration Country : USA
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