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) |
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 |
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) |
27854-170-01 |
27854-170 |
HUMAN OTC DRUG |
AnaDent |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20170123 |
N/A |
ANDA |
ANDA204872 |
Belmora LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (27854-170-01) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
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 |
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) |
79903-005-27 |
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) |
79903-005-30 |
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 |
300 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-30) |
79903-005-75 |
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 |
1 BOTTLE, PLASTIC in 1 CARTON (79903-005-75) / 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
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) |
79903-005-99 |
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 |
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-99) |
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 |
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) |
79903-005-10 |
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 |
1 BOTTLE, PLASTIC in 1 CARTON (79903-005-10) / 40 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
79903-005-12 |
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 |
100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-12) |
51316-817-08 |
51316-817 |
HUMAN OTC DRUG |
Back and Muscle Pain |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220418 |
N/A |
ANDA |
ANDA204872 |
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (51316-817-08) / 24 TABLET, FILM COATED in 1 BOTTLE, PLASTIC |
51316-817-52 |
51316-817 |
HUMAN OTC DRUG |
Back and Muscle Pain |
Naproxen Sodium |
TABLET, FILM COATED |
ORAL |
20220418 |
N/A |
ANDA |
ANDA204872 |
CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (51316-817-52) / 90 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 |