71335-1480-1 |
71335-1480 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
naltrexone hydrochloride |
TABLET, FILM COATED |
ORAL |
20200116 |
N/A |
ANDA |
ANDA076264 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (71335-1480-1) |
71335-1480-2 |
71335-1480 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
naltrexone hydrochloride |
TABLET, FILM COATED |
ORAL |
20200122 |
N/A |
ANDA |
ANDA076264 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
90 TABLET, FILM COATED in 1 BOTTLE (71335-1480-2) |
71335-1480-3 |
71335-1480 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
naltrexone hydrochloride |
TABLET, FILM COATED |
ORAL |
20240530 |
N/A |
ANDA |
ANDA076264 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
60 TABLET, FILM COATED in 1 BOTTLE (71335-1480-3) |
71335-1480-4 |
71335-1480 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
naltrexone hydrochloride |
TABLET, FILM COATED |
ORAL |
20240530 |
N/A |
ANDA |
ANDA076264 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
45 TABLET, FILM COATED in 1 BOTTLE (71335-1480-4) |
71335-1480-5 |
71335-1480 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
naltrexone hydrochloride |
TABLET, FILM COATED |
ORAL |
20240530 |
N/A |
ANDA |
ANDA076264 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
120 TABLET, FILM COATED in 1 BOTTLE (71335-1480-5) |
71335-1480-6 |
71335-1480 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
naltrexone hydrochloride |
TABLET, FILM COATED |
ORAL |
20200910 |
N/A |
ANDA |
ANDA076264 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
15 TABLET, FILM COATED in 1 BOTTLE (71335-1480-6) |
50090-6820-0 |
50090-6820 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
naltrexone hydrochloride |
TABLET, FILM COATED |
ORAL |
20231114 |
N/A |
ANDA |
ANDA076264 |
A-S Medication Solutions |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (50090-6820-0) |
72162-2154-3 |
72162-2154 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
naltrexone hydrochloride |
TABLET, FILM COATED |
ORAL |
20231207 |
N/A |
ANDA |
ANDA076264 |
Bryant Ranch Prepack |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (72162-2154-3) |
68084-291-21 |
68084-291 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
naltrexone hydrochloride |
TABLET, FILM COATED |
ORAL |
20130603 |
N/A |
ANDA |
ANDA076264 |
American Health Packaging |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-291-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-291-11) |
0406-1170-01 |
0406-1170 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
naltrexone hydrochloride |
TABLET, FILM COATED |
ORAL |
20020322 |
N/A |
ANDA |
ANDA076264 |
SpecGx LLC |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
100 TABLET, FILM COATED in 1 BOTTLE (0406-1170-01) |
0406-1170-03 |
0406-1170 |
HUMAN PRESCRIPTION DRUG |
NALTREXONE HYDROCHLORIDE |
naltrexone hydrochloride |
TABLET, FILM COATED |
ORAL |
20020322 |
N/A |
ANDA |
ANDA076264 |
SpecGx LLC |
NALTREXONE HYDROCHLORIDE |
50 mg/1 |
30 TABLET, FILM COATED in 1 BOTTLE (0406-1170-03) |