DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 2DR REDDYS LABS INC
02 1GRANULES
03 1GRANULES INDIA
04 2ABLE
05 3ACTAVIS LABS FL INC
06 1ADAPTIS
07 1AMNEAL PHARMS CO
08 3AMNEAL PHARMS NY
09 2ATNAHS PHARMA US
10 1AUROBINDO PHARMA
11 4AUROBINDO PHARMA LTD
12 2BAYER
13 1BAYER HLTHCARE
14 1BIONPHARMA
15 1CATALENT
16 1CONTRACT PHARMACAL
17 1COREPHARMA
18 2CURRAX
19 3DR REDDYS LABS LTD
20 2GLENMARK PHARMS LTD
21 2HAMILTON PHARMS
22 1HETERO LABS LTD V
23 2HIKMA
24 2IVAX SUB TEVA PHARMS
25 1LNK INTL INC
26 1MARKSANS PHARMA
27 1NOVELGENIX THERAPS
28 1ONESOURCE SPECIALTY
29 1P AND L
30 1PAR PHARM
31 1PATHEON SOFTGELS
32 2PERRIGO
33 1PERRIGO R AND D
34 2PHARMOBEDIENT
35 1PLD ACQUISITIONS LLC
36 2PLIVA
37 1PURACAP PHARM LLC
38 2PUREPAC PHARM
39 1RISING
40 2ROXANE
41 4SANDOZ
42 2SCIEGEN PHARMS INC
43 1SUN PHARM
44 1SUN PHARM INDS LTD
45 4TEVA
46 2TEVA PHARMS
47 3TWI PHARMS
48 4WATSON LABS
49 1YICHANG HUMANWELL
01 5CAPSULE;ORAL
02 10TABLET, EXTENDED RELEASE;ORAL
03 2TABLET; ORAL
04 68TABLET;ORAL
01 41DISCN
02 23OTC
03 19RX
04 2Blank
01 1ALEVE
02 1ALEVE PM
03 1ALEVE-D SINUS & COLD
04 1ANAPROX
05 1ANAPROX DS
06 3NAPRELAN
07 62NAPROXEN SODIUM
08 5NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE
09 3NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE
10 3SUMATRIPTAN AND NAPROXEN SODIUM
11 2SUMATRIPTAN; NAPROXEN SODIUM
12 2TREXIMET
01 72No
02 11Yes
03 2Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code :
Brand Name : NAPROXEN SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : 220MG
Approval Date : 1998-07-28
Application Number : 75168
RX/OTC/DISCN : OTC
RLD : No
TE Code :
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
RLD : No
TE Code :
Brand Name : NAPROXEN SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : 220MG
Approval Date : 2011-09-20
Application Number : 91353
RX/OTC/DISCN : OTC
RLD : No
TE Code :
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
RLD : No
TE Code :
NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE
Brand Name : NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 220MG;120MG
Approval Date : 2006-09-27
Application Number : 77381
RX/OTC/DISCN : OTC
RLD : No
TE Code :
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
RLD : No
TE Code :
DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
Brand Name : NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG;220MG
Approval Date : 2020-09-24
Application Number : 213663
RX/OTC/DISCN : OTC
RLD : No
TE Code :
RLD : Yes
TE Code :
Brand Name : ANAPROX
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 250MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Approval Date : 1982-01-01
Application Number : 18164
RX/OTC/DISCN : DISCN
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Brand Name : ANAPROX DS
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Approval Date : 1987-09-30
Application Number : 18164
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code :
Brand Name : ALEVE
Dosage Form : TABLET;ORAL
Dosage Strength : 220MG
Approval Date : 1994-01-11
Application Number : 20204
RX/OTC/DISCN : OTC
RLD : Yes
TE Code :
RLD : Yes
TE Code : AB
Brand Name : NAPRELAN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 375MG BASE
Approval Date : 1996-01-05
Application Number : 20353
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : NAPRELAN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 500MG BASE
Approval Date : 1996-01-05
Application Number : 20353
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
RLD : Yes
TE Code : AB
Brand Name : NAPRELAN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 750MG BASE
Approval Date : 1996-01-05
Application Number : 20353
RX/OTC/DISCN : RX
RLD : Yes
TE Code : AB
