Please Wait
Applying Filters...
Menu
$ API Ref.Price (USD/KG) : 15Xls
Filters Filter
Cross PopUp
FILTER :

filter clear-filterReset all filters

01 1DR REDDYS

02 1STRIDES PHARMA

03 1ACTAVIS LABS UT INC

04 2ALEMBIC

05 1ALKEM LABS LTD

06 1AMNEAL

07 1AMNEAL PHARMS

08 5ASTRAZENECA

09 1AUROBINDO PHARMA LTD

10 1AVEVA

11 1BELMORA LLC

12 3CARLISLE

13 1COMBE

14 1COSETTE

15 1CRESCITA THERAP

16 1DENTSPLY PHARM

17 2ENCUBE

18 1FOUGERA PHARMS

19 1FOUGERA PHARMS INC

20 1GALEN SPECIALTY

21 1GENEYORK PHARMS

22 1GLENMARK PHARMS LTD

23 1HIKMA

24 2HOFFMANN LA ROCHE

25 1IBSA

26 1MACLEODS PHARMS LTD

27 1NAL PHARM

28 1NORVIUM BIOSCIENCE

29 2NOVEN

30 1NOVEN PHARMS INC

31 1PADAGIS US

32 1PAI HOLDINGS PHARM

33 1QUAGEN

34 1RHODES PHARMS

35 1RISING

36 1SCILEX PHARMS

37 1SEPTODONT INC

38 1TARO

39 1TEIKOKU PHARMA USA

40 1TEVA BRANDED PHARM

41 1TEVA PHARMS USA

42 1VITRUVIAS THERAP

43 1ZYDUS LIFESCIENCES

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

filter clear-filterReset all filters

PharmaCompass

01

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothDRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.

RLD : No

TE Code : AT

LIDOCAINE

Brand Name : LIDOCAINE

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 5%

Approval Date : 2021-01-05

Application Number : 208660

RX/OTC/DISCN : RX

RLD : No

TE Code : AT

Dr Reddy Company Banner

02

  • fda
  • EDQM
  • WHO-GMP

Virtual BoothStrides Pharma Science: Pioneering IP-driven formulations for niche finished dosage forms.

RLD : No

TE Code : AT

LIDOCAINE

Brand Name : LIDOCAINE

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 5%

Approval Date : 2018-12-11

Application Number : 210958

RX/OTC/DISCN : RX

RLD : No

TE Code : AT

Strides Pharma Science

03

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

LIDOCAINE

Brand Name : XYLOCAINE

Dosage Form : OINTMENT;TOPICAL

Dosage Strength : 5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1982-01-01

Application Number : 8048

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank

04

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

LIDOCAINE

Brand Name : XYLOCAINE

Dosage Form : SUPPOSITORY;RECTAL

Dosage Strength : 100MG

Approval Date : 1982-01-01

Application Number : 13077

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

05

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

LIDOCAINE

Brand Name : XYLOCAINE

Dosage Form : SOLUTION;TOPICAL

Dosage Strength : 5%

Approval Date : 1982-01-01

Application Number : 14127

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

06

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

LIDOCAINE

Brand Name : XYLOCAINE

Dosage Form : AEROSOL;ORAL

Dosage Strength : 10%

Approval Date : 1982-01-01

Application Number : 14394

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

07

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

LIDOCAINE

Brand Name : DENTIPATCH

Dosage Form : FILM, EXTENDED RELEASE;BUCCAL

Dosage Strength : 23MG/PATCH

Approval Date : 1996-05-21

Application Number : 20575

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

08

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

LIDOCAINE

Brand Name : DENTIPATCH

Dosage Form : PATCH;TOPICAL

Dosage Strength : 46.1MG/PATCH

Approval Date : 1996-05-21

Application Number : 20575

RX/OTC/DISCN : DISCN

RLD : No

TE Code :

blank

09

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

LIDOCAINE

Brand Name : LIDODERM

Dosage Form : PATCH;TOPICAL

Dosage Strength : 5%

Approval Date : 1999-03-19

Application Number : 20612

RX/OTC/DISCN : RX

RLD : Yes

TE Code : AB

blank

10

AACR Annual meeting
Not Confirmed
arrow
arrow
AACR Annual meeting
Not Confirmed

LIDOCAINE; PRILOCAINE

Brand Name : EMLA

Dosage Form : CREAM;TOPICAL

Dosage Strength : 2.5%;2.5% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**

Approval Date : 1992-12-30

Application Number : 19941

RX/OTC/DISCN : DISCN

RLD : Yes

TE Code :

blank