51991-735-20 |
51991-735 |
HUMAN PRESCRIPTION DRUG |
Granisetron Hydrochloride |
Granisetron Hydrochloride |
TABLET |
ORAL |
20090622 |
N/A |
ANDA |
ANDA078969 |
Breckenridge Pharmaceutical, Inc. |
GRANISETRON HYDROCHLORIDE |
1 mg/1 |
2 BLISTER PACK in 1 CARTON (51991-735-20) / 10 TABLET in 1 BLISTER PACK |
51991-735-32 |
51991-735 |
HUMAN PRESCRIPTION DRUG |
Granisetron Hydrochloride |
Granisetron Hydrochloride |
TABLET |
ORAL |
20090622 |
N/A |
ANDA |
ANDA078969 |
Breckenridge Pharmaceutical, Inc. |
GRANISETRON HYDROCHLORIDE |
1 mg/1 |
1 BLISTER PACK in 1 CARTON (51991-735-32) / 2 TABLET in 1 BLISTER PACK |
63850-0005-1 |
63850-0005 |
HUMAN PRESCRIPTION DRUG |
Granisetron hydrochloride |
Granisetron hydrochloride |
TABLET, FILM COATED |
ORAL |
20090622 |
N/A |
ANDA |
ANDA078969 |
Natco Pharma Limited |
GRANISETRON HYDROCHLORIDE |
1 mg/1 |
10 TABLET, FILM COATED in 1 BLISTER PACK (63850-0005-1) |
63850-0005-2 |
63850-0005 |
HUMAN PRESCRIPTION DRUG |
Granisetron hydrochloride |
Granisetron hydrochloride |
TABLET, FILM COATED |
ORAL |
20090622 |
N/A |
ANDA |
ANDA078969 |
Natco Pharma Limited |
GRANISETRON HYDROCHLORIDE |
1 mg/1 |
2 TABLET, FILM COATED in 1 BLISTER PACK (63850-0005-2) |