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 1NM Pharma Limited
44 2Noripharma
45 1Novelgenix
46 1ONESOURCE SPECIALTY
47 2PHARMOBEDIENT
48 1PL Developments
49 1PLD ACQUISITIONS
50 2PRO DOC LIMITEE
51 1PURACAP PHARM
52 2PUREPAC PHARM
53 1Par Pharmaceutical
54 2Patheon
55 3Perrigo Company plc
56 4Pharmascience Inc.
57 2Pliva Hrvatska
58 2ROXANE
59 1RPG Life Sciences
60 1Rising Pharmaceuticals Inc
61 2SEARCHLIGHT PHARMA
62 4Sandoz B2B
63 2ScieGen Pharmaceuticals
64 1Seoul Pharma Co Ltd
65 4Sun Pharmaceutical Industries Limited
66 2T.M.Thakore Pharmaceutical Laboratories
67 1TAD Pharma
68 3TWi Pharmaceuticals
69 8Teva Pharmaceutical Industries
70 2Umedica Laboratories
71 1Whanin Pharmaceutical
72 2World Medicine
73 3XYZ Pharma
74 2Yichang Humanwell Pharmaceutical
75 2Zim Laboratories
76 1Blank
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 13Film 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
01 1Allowed
02 2Approved
03 1Authorised
04 9Authorized
05 2Cancelled
06 41DISCN
07 3Deregistered
08 11Generic
09 2Lead Market Dossiers- Filed
10 7NON-PRESCRIPTION DRUGS
11 25OTC
12 4Originator
13 9Prescription
14 19RX
15 1TP, ODMF
16 28Blank
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 1Aleve Feminax For Menstrual Pain
15 1Anax
16 1Antalgin
17 1Compresso NAP 73.3
18 1Eox
19 1Ipaflex
20 1MAXIDOL LIQUID GELS
21 1Momen Granules For Oral Solution
22 1NAPOLON
23 3NAPRELAN
24 2NAPROXEN
25 2NAPROXEN MENSTRUAL PAIN RELIEF
26 62NAPROXEN SODIUM
27 5NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE
28 3NAPROXEN SODIUM AND PSEUDOEPHEDRINE HYDROCHLORIDE
29 1NAPROXEN-NA
30 1NAPROXEN-NA DF
31 1NAPROXEN/ESOMEPRAZOLE
32 1Napren S Fort
33 1Naproxen
34 1Naproxen Banner
35 4Naproxen Sodium
36 1Naproxen Sodium Cinfa
37 1Naproxen Sodium Kern Pharma
38 1Naproxen Sodium Tad
39 1Naproxeno Hcs
40 1Naproxeno Sodico Aurovitas
41 1Naproxeno Sodico Normon
42 1Nomigrin
43 1P.P. NAPROXEN NA 275MG TABLET
44 1P.P. NAPROXEN NA 550MG
45 3SUMATRIPTAN AND NAPROXEN SODIUM
46 2SUMATRIPTAN; NAPROXEN SODIUM
47 1SUVEXX
48 1Suvexx
49 4Synax
50 1TEVA-NAPROXEN SODIUM
51 1TEVA-NAPROXEN SODIUM DS
52 2TREXIMET
53 2UPROGESIC
54 21Blank
01 18Canada
02 1China
03 23India
04 2Malaysia
05 1Malta
06 3Poland
07 1Romania
08 4South Africa
09 3South Korea
10 11Spain
11 5Sweden
12 1Switzerland
13 7Turkey
14 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
Synergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.
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
Synergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.
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
Synergice, a Strides Pharma initiative, is a new gen B2B platform for diverse portofolio needs.
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
