| 63941-245-01 |
63941-245 |
HUMAN OTC DRUG |
All Day Pain Relief |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20100610 |
20261130 |
ANDA |
ANDA079096 |
VALU MERCHANDISERS COMPANY |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (63941-245-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 63941-245-02 |
63941-245 |
HUMAN OTC DRUG |
All Day Pain Relief |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20100519 |
20261130 |
ANDA |
ANDA079096 |
VALU MERCHANDISERS COMPANY |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (63941-245-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 63941-245-03 |
63941-245 |
HUMAN OTC DRUG |
All Day Pain Relief |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20100519 |
20270930 |
ANDA |
ANDA079096 |
VALU MERCHANDISERS COMPANY |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (63941-245-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 53943-145-02 |
53943-145 |
HUMAN OTC DRUG |
NAPROXEN |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20141028 |
N/A |
ANDA |
ANDA079096 |
DISCOUNT DRUG MART |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (53943-145-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 53943-145-03 |
53943-145 |
HUMAN OTC DRUG |
NAPROXEN |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20141028 |
N/A |
ANDA |
ANDA079096 |
DISCOUNT DRUG MART |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (53943-145-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 83324-109-01 |
83324-109 |
HUMAN OTC DRUG |
Naproxen Sodium |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20250520 |
N/A |
ANDA |
ANDA079096 |
CHAIN DRUG MARKETING ASSOCIATION, INC. |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 PACKAGE (83324-109-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 83324-109-50 |
83324-109 |
HUMAN OTC DRUG |
Naproxen Sodium |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20250520 |
N/A |
ANDA |
ANDA079096 |
CHAIN DRUG MARKETING ASSOCIATION, INC. |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (83324-109-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 68998-145-03 |
68998-145 |
HUMAN OTC DRUG |
Naproxen Sodium |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20090531 |
N/A |
ANDA |
ANDA079096 |
Marc Glassman, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (68998-145-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 53943-144-02 |
53943-144 |
HUMAN OTC DRUG |
NAPROXEN |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20141028 |
N/A |
ANDA |
ANDA079096 |
DISCOUNT DRUG MART |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (53943-144-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 53943-144-03 |
53943-144 |
HUMAN OTC DRUG |
NAPROXEN |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20141028 |
N/A |
ANDA |
ANDA079096 |
DISCOUNT DRUG MART |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (53943-144-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 83324-108-01 |
83324-108 |
HUMAN OTC DRUG |
Naproxen Sodium |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20250520 |
N/A |
ANDA |
ANDA079096 |
CHAIN DRUG MARKETING ASSOCIATION, INC. |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (83324-108-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 83324-108-24 |
83324-108 |
HUMAN OTC DRUG |
Naproxen Sodium |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20250520 |
N/A |
ANDA |
ANDA079096 |
CHAIN DRUG MARKETING ASSOCIATION, INC. |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (83324-108-24) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 83324-108-50 |
83324-108 |
HUMAN OTC DRUG |
Naproxen Sodium |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20250520 |
N/A |
ANDA |
ANDA079096 |
CHAIN DRUG MARKETING ASSOCIATION, INC. |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (83324-108-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 68998-144-03 |
68998-144 |
HUMAN OTC DRUG |
Naproxen Sodium |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20090601 |
N/A |
ANDA |
ANDA079096 |
Marc Glassman, Inc. |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (68998-144-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 53746-191-05 |
53746-191 |
HUMAN OTC DRUG |
Naproxen Sodium (NSAID) Fever Reducer/ Pain Reliever |
Naproxen Sodium |
TABLET |
ORAL |
20091125 |
N/A |
ANDA |
ANDA079096 |
Amneal Pharmaceuticals of New York LLC |
NAPROXEN SODIUM |
220 mg/1 |
500 TABLET in 1 BOTTLE (53746-191-05) |
| 53746-191-08 |
53746-191 |
HUMAN OTC DRUG |
Naproxen Sodium (NSAID) Fever Reducer/ Pain Reliever |
Naproxen Sodium |
TABLET |
ORAL |
20091125 |
N/A |
ANDA |
ANDA079096 |
Amneal Pharmaceuticals of New York LLC |
NAPROXEN SODIUM |
220 mg/1 |
8 TABLET in 1 VIAL (53746-191-08) |
| 50090-2388-0 |
50090-2388 |
HUMAN OTC DRUG |
Medique Mediproxen |
NAPROXEN SODIUM |
TABLET, FILM COATED |
ORAL |
20160428 |
N/A |
ANDA |
ANDA079096 |
A-S Medication Solutions |
NAPROXEN SODIUM |
220 mg/1 |
100 PACKET in 1 BOX, UNIT-DOSE (50090-2388-0) / 1 TABLET, FILM COATED in 1 PACKET |
| 63868-466-01 |
63868-466 |
HUMAN OTC DRUG |
Naproxen Sodium |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20090619 |
20280131 |
ANDA |
ANDA079096 |
Chain Drug Marketing Association |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (63868-466-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 63868-466-25 |
63868-466 |
HUMAN OTC DRUG |
Naproxen Sodium |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20130502 |
20270930 |
ANDA |
ANDA079096 |
Chain Drug Marketing Association |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (63868-466-25) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 63868-466-50 |
63868-466 |
HUMAN OTC DRUG |
Naproxen Sodium |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20090619 |
20270930 |
ANDA |
ANDA079096 |
Chain Drug Marketing Association |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (63868-466-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC |