| 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) |
| 53746-191-24 |
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 |
24 TABLET in 1 BOTTLE (53746-191-24) |
| 53746-192-05 |
53746-192 |
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 (53746-192-05) |
| 53746-192-08 |
53746-192 |
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 (53746-192-08) |
| 53746-192-24 |
53746-192 |
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 |
24 TABLET in 1 BOTTLE (53746-192-24) |
| 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 |
| 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 |
| 59726-169-15 |
59726-169 |
HUMAN OTC DRUG |
All Day Pain Relief |
Naproxen sodium |
TABLET |
ORAL |
20140228 |
N/A |
ANDA |
ANDA079096 |
P & L Development, LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 BOX (59726-169-15) / 15 TABLET in 1 BOTTLE, PLASTIC |
| 59726-169-40 |
59726-169 |
HUMAN OTC DRUG |
All Day Pain Relief |
Naproxen sodium |
TABLET |
ORAL |
20140228 |
N/A |
ANDA |
ANDA079096 |
P & L Development, LLC |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 BOX (59726-169-40) / 40 TABLET in 1 BOTTLE, PLASTIC |
| 63868-465-01 |
63868-465 |
HUMAN OTC DRUG |
Naproxen Sodium |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20090903 |
20271231 |
ANDA |
ANDA079096 |
Chain Drug Marketing Association |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (63868-465-01) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 63868-465-50 |
63868-465 |
HUMAN OTC DRUG |
Naproxen Sodium |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20090903 |
20271231 |
ANDA |
ANDA079096 |
Chain Drug Marketing Association |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (63868-465-50) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 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 |
| 63941-144-01 |
63941-144 |
HUMAN OTC DRUG |
All Day Pain Relief |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20100629 |
20261031 |
ANDA |
ANDA079096 |
VALU MERCHANDISERS COMPANY |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (63941-144-01) / 24 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 63941-144-02 |
63941-144 |
HUMAN OTC DRUG |
All Day Pain Relief |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20100610 |
20261031 |
ANDA |
ANDA079096 |
VALU MERCHANDISERS COMPANY |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (63941-144-02) / 50 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 63941-144-03 |
63941-144 |
HUMAN OTC DRUG |
All Day Pain Relief |
NAPROXEN SODIUM |
TABLET, COATED |
ORAL |
20100803 |
20261031 |
ANDA |
ANDA079096 |
VALU MERCHANDISERS COMPANY |
NAPROXEN SODIUM |
220 mg/1 |
1 BOTTLE, PLASTIC in 1 CARTON (63941-144-03) / 100 TABLET, COATED in 1 BOTTLE, PLASTIC |
| 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 |