| 21130-856-52 |
21130-856 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20231011 |
N/A |
ANDA |
ANDA204872 |
Better Living Brands, LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (21130-856-52) / 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 71335-1282-1 |
71335-1282 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20211118 |
N/A |
ANDA |
ANDA204872 |
Bryant Ranch Prepack |
NAPROXEN SODIUM |
220 mg/1 |
20 TABLET in 1 BOTTLE (71335-1282-1) |
| 71335-1282-2 |
71335-1282 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20190827 |
N/A |
ANDA |
ANDA204872 |
Bryant Ranch Prepack |
NAPROXEN SODIUM |
220 mg/1 |
30 TABLET in 1 BOTTLE (71335-1282-2) |
| 71335-1282-3 |
71335-1282 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20191022 |
N/A |
ANDA |
ANDA204872 |
Bryant Ranch Prepack |
NAPROXEN SODIUM |
220 mg/1 |
40 TABLET in 1 BOTTLE (71335-1282-3) |
| 71335-1282-4 |
71335-1282 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20250110 |
N/A |
ANDA |
ANDA204872 |
Bryant Ranch Prepack |
NAPROXEN SODIUM |
220 mg/1 |
50 TABLET in 1 BOTTLE (71335-1282-4) |
| 71335-1282-5 |
71335-1282 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20250130 |
N/A |
ANDA |
ANDA204872 |
Bryant Ranch Prepack |
NAPROXEN SODIUM |
220 mg/1 |
60 TABLET in 1 BOTTLE (71335-1282-5) |
| 71335-1282-6 |
71335-1282 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20191126 |
N/A |
ANDA |
ANDA204872 |
Bryant Ranch Prepack |
NAPROXEN SODIUM |
220 mg/1 |
14 TABLET in 1 BOTTLE (71335-1282-6) |
| 71335-1282-7 |
71335-1282 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20191025 |
N/A |
ANDA |
ANDA204872 |
Bryant Ranch Prepack |
NAPROXEN SODIUM |
220 mg/1 |
100 TABLET in 1 BOTTLE (71335-1282-7) |
| 71335-1282-8 |
71335-1282 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20250130 |
N/A |
ANDA |
ANDA204872 |
Bryant Ranch Prepack |
NAPROXEN SODIUM |
220 mg/1 |
90 TABLET in 1 BOTTLE (71335-1282-8) |
| 11822-4170-5 |
11822-4170 |
HUMAN OTC DRUG |
Back and Muscle Pain |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220707 |
N/A |
ANDA |
ANDA204872 |
Rite Aid Corporation |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (11822-4170-5) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 27854-165-10 |
27854-165 |
HUMAN OTC DRUG |
Flanax Menstrual Pain Reliever |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20170123 |
N/A |
ANDA |
ANDA204872 |
Belmora LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (27854-165-10) / 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 55319-406-15 |
55319-406 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20231215 |
N/A |
ANDA |
ANDA204872 |
Family Dollar Services Inc |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (55319-406-15) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 79903-005-20 |
79903-005 |
HUMAN OTC DRUG |
All Day Pain Relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20201022 |
N/A |
ANDA |
ANDA204872 |
WALMART INC. |
NAPROXEN SODIUM |
220 mg/1 |
200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-20) |
| 79903-005-25 |
79903-005 |
HUMAN OTC DRUG |
All Day Pain Relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20201022 |
N/A |
ANDA |
ANDA204872 |
WALMART INC. |
NAPROXEN SODIUM |
220 mg/1 |
225 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-25) |
| 79903-005-27 |
79903-005 |
HUMAN OTC DRUG |
All Day Pain Relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20201022 |
N/A |
ANDA |
ANDA204872 |
WALMART INC. |
NAPROXEN SODIUM |
220 mg/1 |
270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27) |
| 79903-005-90 |
79903-005 |
HUMAN OTC DRUG |
All Day Pain Relief |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20201022 |
N/A |
ANDA |
ANDA204872 |
WALMART INC. |
NAPROXEN SODIUM |
220 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-90) |
| 50844-417-11 |
50844-417 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20170201 |
N/A |
ANDA |
ANDA204872 |
L.N.K. International, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
60 POUCH in 1 CARTON (50844-417-11) / 1 TABLET, FILM COATED in 1 POUCH (50844-417-43) |
| 42961-122-02 |
42961-122 |
HUMAN OTC DRUG |
First Aid Direct All Day Pain Relief |
Naproxen Sodium |
TABLET, COATED |
ORAL |
20230719 |
N/A |
ANDA |
ANDA204872 |
Cintas Corporation |
NAPROXEN SODIUM |
220 mg/1 |
25 PACKET in 1 BOX (42961-122-02) / 1 TABLET, COATED in 1 PACKET (42961-122-01) |
| 27854-160-01 |
27854-160 |
HUMAN OTC DRUG |
Flanax |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20180115 |
N/A |
ANDA |
ANDA204872 |
Belmora LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (27854-160-01) / 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 27854-160-24 |
27854-160 |
HUMAN OTC DRUG |
Flanax |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20180115 |
N/A |
ANDA |
ANDA204872 |
Belmora LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (27854-160-24) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |