| 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) |
| 71335-1282-9 |
71335-1282 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20250130 |
N/A |
ANDA |
ANDA204872 |
Bryant Ranch Prepack |
NAPROXEN SODIUM |
220 mg/1 |
24 TABLET in 1 BOTTLE (71335-1282-9) |
| 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 |
| 68071-5039-1 |
68071-5039 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20230110 |
N/A |
ANDA |
ANDA204872 |
NuCare Pharmaceuticals,Inc. |
NAPROXEN SODIUM |
220 mg/1 |
21 TABLET in 1 BOTTLE (68071-5039-1) |
| 68788-7572-2 |
68788-7572 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20191227 |
N/A |
ANDA |
ANDA204872 |
Preferred Pharmaceuticals, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
20 TABLET in 1 BOTTLE (68788-7572-2) |
| 68788-7572-3 |
68788-7572 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20191227 |
N/A |
ANDA |
ANDA204872 |
Preferred Pharmaceuticals, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
30 TABLET in 1 BOTTLE (68788-7572-3) |
| 68788-7572-4 |
68788-7572 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20191227 |
N/A |
ANDA |
ANDA204872 |
Preferred Pharmaceuticals, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
40 TABLET in 1 BOTTLE (68788-7572-4) |
| 68788-7572-6 |
68788-7572 |
HUMAN OTC DRUG |
Naproxen |
Naproxen Sodium |
TABLET |
ORAL |
20191227 |
N/A |
ANDA |
ANDA204872 |
Preferred Pharmaceuticals, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
60 TABLET in 1 BOTTLE (68788-7572-6) |
| 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 |
| 50844-604-06 |
50844-604 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20260219 |
N/A |
ANDA |
ANDA204872 |
L.N.K. International, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
200 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-06) |
| 50844-604-09 |
50844-604 |
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 |
4 BLISTER PACK in 1 CARTON (50844-604-09) / 5 TABLET, FILM COATED in 1 BLISTER PACK |
| 50844-604-14 |
50844-604 |
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 |
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-604-14) |
| 11822-6040-5 |
11822-6040 |
HUMAN OTC DRUG |
Naproxen Sodium |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220718 |
N/A |
ANDA |
ANDA204872 |
Rite Aid Corporation |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (11822-6040-5) / 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
| 50844-714-14 |
50844-714 |
HUMAN OTC DRUG |
Naproxen Back and Muscle Pain |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20190201 |
N/A |
ANDA |
ANDA204872 |
L.N.K. International, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-14) |
| 50844-714-16 |
50844-714 |
HUMAN OTC DRUG |
Naproxen Back and Muscle Pain |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20190201 |
N/A |
ANDA |
ANDA204872 |
L.N.K. International, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50844-714-16) |
| 50844-714-19 |
50844-714 |
HUMAN OTC DRUG |
Naproxen Back and Muscle Pain |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20190201 |
N/A |
ANDA |
ANDA204872 |
L.N.K. International, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (50844-714-19) / 8 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |