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01 2Orion Corporation
02 4Dr. Reddy's Laboratories
03 3Strides Pharma Science
04 4Granules India Limited
05 1ADAPTIS
06 3ATNAHS PHARMA UK LIMITED
07 7Actavis Inc
08 3Adamed Pharma
09 1Aeon Formulations Private Limited
10 4Amneal Pharmaceuticals
11 1Angelini Pharma
12 1Antibiotice
13 2Apotex Inc
14 1Aralez Pharmaceuticals
15 1Ascent Innovative Medicines
16 5Aurobindo Pharma Limited
17 1Aurovitas Spain, Sau
18 16Bayer AG
19 4Biofarma Pharmaceutical Industry and Commerce Inc
20 1Bionpharma
21 1Catalent Pharma Solutions
22 1Cinfa
23 1Contract Pharmacal Corporation
24 1CorePharma, LLC
25 2Currax
26 2Glenmark Pharmaceuticals
27 1Grup Farma
28 1HCS Bvba
29 2Hamilton
30 1Hetero Drugs
31 2Hikma Pharmaceuticals
32 1Holden Medical Laboratories Pvt. Ltd
33 2IVAX Pharmaceuticals Inc
34 1Johnson & Johnson
35 1Kern Pharma S.L.
36 1LABORATORIOS NORMON SA
37 1LNK
38 1Madras Pharmaceuticals
39 1Marksans Pharma
40 4Mars Therapeutics
41 1Meda Otc Ab
42 1Myungmoon Pharm. Co., LTD.
43 2Noripharma
44 1Novelgenix
45 1ONESOURCE SPECIALTY
46 2PHARMOBEDIENT
47 1PL Developments
48 1PLD ACQUISITIONS
49 2PRO DOC LIMITEE
50 1PURACAP PHARM
51 2PUREPAC PHARM
52 1Par Pharmaceutical
53 2Patheon
54 3Perrigo Company plc
55 4Pharmascience Inc.
56 2Pliva Hrvatska
57 2ROXANE
58 1RPG Life Sciences
59 1Rising Pharmaceuticals Inc
60 2SEARCHLIGHT PHARMA
61 4Sandoz B2B
62 2ScieGen Pharmaceuticals
63 1Seoul Pharma Co Ltd
64 4Sun Pharmaceutical Industries Limited
65 2T.M.Thakore Pharmaceutical Laboratories
66 1TAD Pharma
67 3TWi Pharmaceuticals
68 8Teva Pharmaceutical Industries
69 2Umedica Laboratories
70 1Whanin Pharmaceutical
71 2World Medicine
72 3XYZ Pharma
73 2Yichang Humanwell Pharmaceutical
74 2Zim Laboratories
75 1Blank
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01 1BILAYERED TABLET
02 2CAP
03 3CAPSULE
04 5CAPSULE;ORAL
05 3Capsule
06 3DC Granules
07 2DC Granules and Tablets
08 2ENTERIC COATED TABLETS
09 4FC Tablet
10 2FILM COATED TABLET
11 12Film Coated Tablet
12 2Film-Coated Tablet
13 1Immediate Release Tablet
14 1Modified Release Tablet
15 2Oral Solid Dosage Form
16 1Oral Solution
17 1Soft Gel
18 1Soft Gel Capsule
19 2Softgelatin Capsule
20 2TAB
21 20TABLET
22 10TABLET, EXTENDED RELEASE;ORAL
23 2TABLET; ORAL
24 68TABLET;ORAL
25 10Tablet
26 1modi?ed-release tablets
27 1Blank
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01 1Allowed
02 2Approved
03 9Authorized
04 2Cancelled
05 41DISCN
06 3Deregistered
07 11Generic
08 2Lead Market Dossiers- Filed
09 7NON-PRESCRIPTION DRUGS
10 25OTC
11 4Originator
12 9Prescription
13 19RX
14 1TP, ODMF
15 28Blank
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01 1ALEVE
02 1ALEVE BACK AND BODY PAIN
03 1ALEVE CAPLETS
04 1ALEVE LIQUID GELS
05 1ALEVE NIGHTTIME
06 1ALEVE PM
07 1ALEVE-D SINUS & COLD
08 2ANAPROX
09 2ANAPROX DS
10 1APO-NAPRO-NA
11 1APO-NAPRO-NA DS
12 1Actromadol
13 8Aleve
14 1Anax
15 1Antalgin
16 1Compresso NAP 73.3
17 1Eox
18 1Ipaflex
19 1MAXIDOL LIQUID GELS
20 1Momen Granules For Oral Solution
21 1NAPOLON
22 3NAPRELAN
23 2NAPROXEN
24 2NAPROXEN MENSTRUAL PAIN RELIEF
25 62NAPROXEN SODIUM
26 5NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE
27 3NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE
28 1NAPROXEN-NA
29 1NAPROXEN-NA DF
30 1NAPROXEN/ESOMEPRAZOLE
31 1Napren S Fort
32 1Naproxen
33 1Naproxen Banner
34 4Naproxen Sodium
35 1Naproxen Sodium Cinfa
36 1Naproxen Sodium Kern Pharma
37 1Naproxen Sodium Tad
38 1Naproxeno Hcs
39 1Naproxeno Sodico Aurovitas
40 1Naproxeno Sodico Normon
41 1Nomigrin
42 1P.P. NAPROXEN NA 275MG TABLET
43 1P.P. NAPROXEN NA 550MG
44 3SUMATRIPTAN AND NAPROXEN SODIUM
45 2SUMATRIPTAN; NAPROXEN SODIUM
46 1SUVEXX
47 1Suvexx
48 4Synax
49 1TEVA-NAPROXEN SODIUM
50 1TEVA-NAPROXEN SODIUM DS
51 2TREXIMET
52 2UPROGESIC
53 21Blank
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01 18Canada
02 1China
03 23India
04 2Malaysia
05 3Poland
06 1Romania
07 4South Africa
08 3South Korea
09 11Spain
10 5Sweden
11 1Switzerland
12 7Turkey
13 85USA
Regulatory Info : Approved
Registration Country : Sweden
Naproxen Sodium; Sumatriptan Succinate
Brand Name : Nomigrin
Dosage Form : Film Coated Tablet
Dosage Strength : 85mg;457mg
Packaging :
Approval Date : 21/06/2022
Application Number : 20210104000057
Regulatory Info : Approved
Registration Country : Sweden
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : OTC
Registration Country : USA
Brand Name : NAPROXEN SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : 220MG
Packaging :
Approval Date : 1998-07-28
Application Number : 75168
Regulatory Info : OTC
Registration Country : USA
Regulatory Info :
Registration Country : India
Brand Name : Naproxen Sodium
Dosage Form : Tablet
Dosage Strength : 250MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Regulatory Info : OTC
Registration Country : USA
Brand Name : NAPROXEN SODIUM
Dosage Form : TABLET;ORAL
Dosage Strength : 220MG
Packaging :
Approval Date : 2011-09-20
Application Number : 91353
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : Authorized
Registration Country : Spain
Naproxene Sodium; Sumatriptan Succinate
Brand Name : Suvexx
Dosage Form : Film Coated Tablet
Dosage Strength : 85MG; 500 MG
Packaging :
Approval Date : 2025-04-10
Application Number : 89272
Regulatory Info : Authorized
Registration Country : Spain
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : OTC
Registration Country : USA
NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE
Brand Name : NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 220MG;120MG
Packaging :
Approval Date : 2006-09-27
Application Number : 77381
Regulatory Info : OTC
Registration Country : USA
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
Esomeprazole Magnesium; Naproxen Sodium
Brand Name :
Dosage Form : Oral Solid Dosage Form
Dosage Strength : 20MG; 375MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
Esomeprazole Magnesium; Naproxen Sodium
Brand Name :
Dosage Form : Oral Solid Dosage Form
Dosage Strength : 20MG; 500MG
Packaging :
Approval Date :
Application Number :
Regulatory Info : Lead Market Dossiers- Filed
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name : Naproxen Sodium
Dosage Form : Tablet
Dosage Strength : 500MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Regulatory Info :
Registration Country : India
Brand Name : Naproxen Sodium
Dosage Form : Soft Gel Capsule
Dosage Strength : 220MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Regulatory Info : OTC
Registration Country : USA
DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM
Brand Name : NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE
Dosage Form : TABLET;ORAL
Dosage Strength : 25MG;220MG
Packaging :
Approval Date : 2020-09-24
Application Number : 213663
Regulatory Info : OTC
Registration Country : USA
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Regulatory Info :
Registration Country : India
Brand Name : Naproxen Sodium
Dosage Form : Immediate Release Tablet
Dosage Strength : 220MG
Packaging :
Approval Date :
Application Number :
Regulatory Info :
Registration Country : India
Granules India Limited has high volume world-class facilities for APIs, PFIs, & FDFs, serving customers in over 80 countries.
Regulatory Info : TP, ODMF
Registration Country : India
Brand Name : Compresso NAP 73.3
Dosage Form :
Dosage Strength : 73.3%
Packaging :
Approval Date :
Application Number :
Regulatory Info : TP, ODMF
Registration Country : India
Regulatory Info : DISCN
Registration Country : USA
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**
Packaging :
Approval Date : 1982-01-01
Application Number : 18164
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : ANAPROX DS
Dosage Form : TABLET;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1987-09-30
Application Number : 18164
Regulatory Info : RX
Registration Country : USA
Regulatory Info : OTC
Registration Country : USA
Brand Name : ALEVE
Dosage Form : TABLET;ORAL
Dosage Strength : 220MG
Packaging :
Approval Date : 1994-01-11
Application Number : 20204
Regulatory Info : OTC
Registration Country : USA
Regulatory Info : DISCN
Registration Country : USA
NAPROXEN SODIUM; PSEUDOEPHEDRINE HYDROCHLORIDE
Brand Name : ALEVE-D SINUS & COLD
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : 220MG;120MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Packaging :
Approval Date : 1999-11-29
Application Number : 21076
Regulatory Info : DISCN
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NAPRELAN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 375MG BASE
Packaging :
Approval Date : 1996-01-05
Application Number : 20353
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NAPRELAN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 500MG BASE
Packaging :
Approval Date : 1996-01-05
Application Number : 20353
Regulatory Info : RX
Registration Country : USA
Regulatory Info : RX
Registration Country : USA
Brand Name : NAPRELAN
Dosage Form : TABLET, EXTENDED RELEASE;ORAL
Dosage Strength : EQ 750MG BASE
Packaging :
Approval Date : 1996-01-05
Application Number : 20353
Regulatory Info : RX
Registration Country : USA