72162-1566-1 |
72162-1566 |
HUMAN PRESCRIPTION DRUG |
Naltrexone Hydrochloride |
Naltrexone Hydrochloride |
TABLET, FILM COATED |
ORAL |
20230912 |
N/A |
ANDA |
ANDA075274 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (72162-1566-1) |
72162-1566-3 |
72162-1566 |
HUMAN PRESCRIPTION DRUG |
Naltrexone Hydrochloride |
Naltrexone Hydrochloride |
TABLET, FILM COATED |
ORAL |
20230912 |
N/A |
ANDA |
ANDA075274 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (72162-1566-3) |
63629-1046-1 |
63629-1046 |
HUMAN PRESCRIPTION DRUG |
Naltrexone Hydrochloride |
Naltrexone Hydrochloride |
TABLET, FILM COATED |
ORAL |
20190701 |
N/A |
ANDA |
ANDA075274 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (63629-1046-1) |
63629-1047-1 |
63629-1047 |
HUMAN PRESCRIPTION DRUG |
Naltrexone Hydrochloride |
Naltrexone Hydrochloride |
TABLET, FILM COATED |
ORAL |
20190701 |
N/A |
ANDA |
ANDA075274 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (63629-1047-1) |
68094-853-62 |
68094-853 |
HUMAN PRESCRIPTION DRUG |
Naltrexone Hydrochloride |
naltrexone Hydrochloride |
TABLET, FILM COATED |
ORAL |
20141029 |
N/A |
ANDA |
ANDA075274 |
Precision Dose Inc. |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
3 BLISTER PACK in 1 CARTON (68094-853-62) / 10 TABLET, FILM COATED in 1 BLISTER PACK |
68094-909-30 |
68094-909 |
HUMAN PRESCRIPTION DRUG |
Naltrexone Hydrochloride |
Naltrexone Hydrochloride |
TABLET, FILM COATED |
ORAL |
20240215 |
N/A |
ANDA |
ANDA075274 |
Precision Dose Inc. |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (68094-909-30) |
68094-909-50 |
68094-909 |
HUMAN PRESCRIPTION DRUG |
Naltrexone Hydrochloride |
Naltrexone Hydrochloride |
TABLET, FILM COATED |
ORAL |
20240215 |
N/A |
ANDA |
ANDA075274 |
Precision Dose Inc. |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (68094-909-50) |
51224-206-30 |
51224-206 |
HUMAN PRESCRIPTION DRUG |
Naltrexone Hydrochloride |
Naltrexone Hydrochloride |
TABLET, FILM COATED |
ORAL |
20130923 |
N/A |
ANDA |
ANDA075274 |
TAGI Pharma Inc. |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (51224-206-30) |
51224-206-50 |
51224-206 |
HUMAN PRESCRIPTION DRUG |
Naltrexone Hydrochloride |
Naltrexone Hydrochloride |
TABLET, FILM COATED |
ORAL |
20130923 |
N/A |
ANDA |
ANDA075274 |
TAGI Pharma Inc. |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (51224-206-50) |
42291-632-30 |
42291-632 |
HUMAN PRESCRIPTION DRUG |
Naltrexone Hydrochloride |
Naltrexone Hydrochloride |
TABLET, FILM COATED |
ORAL |
20150326 |
N/A |
ANDA |
ANDA075274 |
AvKARE |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (42291-632-30) |