71335-2062-1 |
71335-2062 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
NALTREXONE HYDROCHLORIDE |
TABLET, FILM COATED |
ORAL |
20220321 |
N/A |
ANDA |
ANDA090356 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (71335-2062-1) |
71335-2062-2 |
71335-2062 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
NALTREXONE HYDROCHLORIDE |
TABLET, FILM COATED |
ORAL |
20220321 |
N/A |
ANDA |
ANDA090356 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (71335-2062-2) |
71335-2062-3 |
71335-2062 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
NALTREXONE HYDROCHLORIDE |
TABLET, FILM COATED |
ORAL |
20220321 |
N/A |
ANDA |
ANDA090356 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (71335-2062-3) |
71335-2062-4 |
71335-2062 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
NALTREXONE HYDROCHLORIDE |
TABLET, FILM COATED |
ORAL |
20220321 |
N/A |
ANDA |
ANDA090356 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
45 TABLET, FILM COATED in 1 BOTTLE (71335-2062-4) |
71335-2062-5 |
71335-2062 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
NALTREXONE HYDROCHLORIDE |
TABLET, FILM COATED |
ORAL |
20220321 |
N/A |
ANDA |
ANDA090356 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE (71335-2062-5) |
71335-2062-6 |
71335-2062 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
NALTREXONE HYDROCHLORIDE |
TABLET, FILM COATED |
ORAL |
20220321 |
N/A |
ANDA |
ANDA090356 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
15 TABLET, FILM COATED in 1 BOTTLE (71335-2062-6) |
0904-7036-04 |
0904-7036 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
NALTREXONE HYDROCHLORIDE |
TABLET, FILM COATED |
ORAL |
20120229 |
N/A |
ANDA |
ANDA090356 |
Major Pharmaceuticals |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 BLISTER PACK in 1 CARTON (0904-7036-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK |
47335-326-08 |
47335-326 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
NALTREXONE HYDROCHLORIDE |
TABLET, FILM COATED |
ORAL |
20120229 |
N/A |
ANDA |
ANDA090356 |
Sun Pharmaceutical Industries, Inc. |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (47335-326-08) |
47335-326-18 |
47335-326 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
NALTREXONE HYDROCHLORIDE |
TABLET, FILM COATED |
ORAL |
20120229 |
N/A |
ANDA |
ANDA090356 |
Sun Pharmaceutical Industries, Inc. |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
1000 TABLET, FILM COATED in 1 BOTTLE (47335-326-18) |
47335-326-83 |
47335-326 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
NALTREXONE HYDROCHLORIDE |
TABLET, FILM COATED |
ORAL |
20120229 |
N/A |
ANDA |
ANDA090356 |
Sun Pharmaceutical Industries, Inc. |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (47335-326-83) |
47335-326-88 |
47335-326 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
NALTREXONE HYDROCHLORIDE |
TABLET, FILM COATED |
ORAL |
20120229 |
N/A |
ANDA |
ANDA090356 |
Sun Pharmaceutical Industries, Inc. |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (47335-326-88) |