01 3Aspen Pharmacare Holdings
02 1Dr. Reddy's Laboratories
03 6Strides Pharma Science
04 2AAIPharma Services Corp.
05 3Actavis Inc
06 8Alkem Laboratories
07 1Alphapharm PTY Ltd
08 3Alvogen
09 4Ascent Innovative Medicines
10 14Aurobindo Pharma Limited
11 2Avva Rus JSC
12 7Barr Laboratories
13 12Bausch & Lomb Incorporated
14 3Beximco Pharmaceuticals
15 4Chartwell Pharmaceuticals llc
16 2EPI Health
17 1Hainan Haiyao
18 1Health Biotech
19 2Hiral Labs
20 6Impax Laboratories
21 7JMC Corporation KR
22 1Kaliberr Labs
23 1Kolmar Korea Co., Ltd.
24 1Leading Pharma, LLC
25 3NORVIUM BIOSCIENCE
26 1Nexus Pharmaceuticals
27 1ORA PHARMA INC.
28 1ORAPHARMA
29 1OraPharma Inc.
30 4Pharmascience Inc.
31 1Protect Life Sciences
32 1REMPEX PHARMS INC
33 5Rising Pharmaceuticals Inc
34 12Sandoz B2B
35 21Sun Pharmaceutical Industries Limited
36 2TEOFARMA Srl
37 4TRIAX PHARMS
38 2Titan Laboratories
39 6Torrent Pharmaceuticals Limited
40 2Wellcopharma
41 3XYZ Pharma
42 3Zydus Lifesciences
43 8Zydus Pharmaceuticals
01 2AEROSOL, FOAM;TOPICAL
02 2CAP
03 6CAPSULE
04 6CAPSULE, EXTENDED RELEASE;ORAL
05 26CAPSULE;ORAL
06 6Capsule
07 1Dental Ointment
08 4ER Tablet
09 2Film Coated Tablet
10 3INJECTABLE;INJECTION
11 2Injection
12 1Minocycline 100Mg 8 Joined' Oral Use
13 1PERIODONTALPULVER
14 1POWDER (EXTENDED RELEASE)
15 1POWDER, EXTENDED RELEASE;DENTAL
16 1SUSPENSION;ORAL
17 4TAB
18 3TABLET, EXTENDED RELEASE; ORAL
19 74TABLET, EXTENDED RELEASE;ORAL
20 20TABLET;ORAL
21 4Tablet
22 2Tablet, Extended Release; Oral
23 1Vial
24 2tablet
25 1Blank
01 61DISCN
02 6Generic
03 7Prescription
04 70RX
05 32Blank
01 1AMZEEQ
02 1ARESTIN
03 1ARESTIN MICROSPHERES
04 1Akamin 50
05 1Arestin
06 2Cyclimycin
07 3DYNACIN
08 1EMROSI
09 8MINOCIN
10 2MINOCYCLINE
11 108MINOCYCLINE HYDROCHLORIDE
12 2MINOLIRA
13 2Minac
14 1Minapro
15 2Minocin
16 2Minolexin
17 1Minomycin-50
18 1Minotabs 50
19 4PMS-MINOCYCLINE
20 8SOLODYN
21 3Sandoz Minocycline
22 1Treaton Dental Ointmentment
23 5XIMINO
24 1ZILXI
25 14Blank
01 2Australia
02 7Canada
03 1China
04 2Guatemala
05 14India
06 2Italy
07 2Russia
08 6South Africa
09 1South Korea
10 1Sweden
11 138USA
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Cyclimycin
Dosage Form : CAP
Dosage Strength : 50mg
Packaging : 60X1mg
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 : EMROSI
Dosage Form : CAPSULE, EXTENDED RELEASE;ORAL
Dosage Strength : 40MG
Packaging :
Approval Date :
Application Number : 219015
Regulatory Info :
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : RX
Registration Country : USA
Brand Name : MINOCYCLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 50MG BASE
Packaging :
Approval Date : 2003-04-16
Application Number : 65131
Regulatory Info : RX
Registration Country : USA
Regulatory Info : Generic
Registration Country : South Africa
Brand Name : Cyclimycin
Dosage Form : CAP
Dosage Strength : 100mg
Packaging : 100X1mg
Approval Date :
Application Number :
Regulatory Info : Generic
Registration Country : South Africa
Regulatory Info :
Registration Country : Australia
Brand Name : Minomycin-50
Dosage Form : tablet
Dosage Strength : 50 mg
Packaging : 60
Approval Date :
Application Number :
Regulatory Info :
Registration Country : Australia
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : RX
Registration Country : USA
Brand Name : MINOCYCLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 75MG BASE
Packaging :
Approval Date : 2003-04-16
Application Number : 65131
Regulatory Info : RX
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info : RX
Registration Country : USA
Brand Name : MINOCYCLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 100MG BASE
Packaging :
Approval Date : 2003-04-16
Application Number : 65131
Regulatory Info : RX
Registration Country : USA
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 50MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 75MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Strides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.
Regulatory Info :
Registration Country : India
Brand Name :
Dosage Form : Tablet
Dosage Strength : 100MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MINOCIN
Dosage Form : SUSPENSION;ORAL
Dosage Strength : EQ 50MG BASE/5ML
Packaging :
Approval Date : 1982-01-01
Application Number : 50445
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MINOCIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 50MG BASE
Packaging :
Approval Date : 1990-05-31
Application Number : 50649
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MINOCIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 100MG BASE
Packaging :
Approval Date : 1990-05-31
Application Number : 50649
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MINOCIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 75MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2001-02-12
Application Number : 50649
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOLODYN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 45MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2006-05-08
Application Number : 50808
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOLODYN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 90MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2006-05-08
Application Number : 50808
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOLODYN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 135MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 2006-05-08
Application Number : 50808
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOLODYN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 65MG BASE
Packaging :
Approval Date : 2009-07-23
Application Number : 50808
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOLODYN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 115MG BASE
Packaging :
Approval Date : 2009-07-23
Application Number : 50808
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOLODYN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 105MG BASE
Packaging :
Approval Date : 2010-08-27
Application Number : 50808
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOLODYN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 80MG BASE
Packaging :
Approval Date : 2010-08-27
Application Number : 50808
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : SOLODYN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 55MG BASE
Packaging :
Approval Date : 2010-08-27
Application Number : 50808
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MINOCIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 100MG BASE/VIAL
Packaging :
Approval Date : 1982-01-01
Application Number : 62139
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ARESTIN
Dosage Form : POWDER, EXTENDED RELEASE;DENTAL
Dosage Strength : EQ 1MG BASE
Packaging :
Approval Date : 2001-02-16
Application Number : 50781
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MINOCIN
Dosage Form : INJECTABLE;INJECTION
Dosage Strength : EQ 100MG BASE/VIAL
Packaging :
Approval Date : 1982-01-01
Application Number : 50444
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : MINOCYCLINE HYDROCHLORIDE
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 100MG BASE
Packaging :
Approval Date : 1992-03-02
Application Number : 63009
Regulatory Info : RX
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MINOCIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 100MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 50315
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MINOCIN
Dosage Form : CAPSULE;ORAL
Dosage Strength : EQ 50MG BASE
Packaging :
Approval Date : 1982-01-01
Application Number : 50315
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MINOCYCLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 100MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-08-10
Application Number : 50451
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
Regulatory Info : DISCN
Registration Country : USA
Brand Name : MINOCYCLINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 50MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1982-08-10
Application Number : 50451
Regulatory Info : DISCN
Registration Country : USA
Portfolio PDF
Product Web Link
Virtual Booth
Digital Content
Website
Corporate PDF
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