68462-521-01 |
68462-521 |
HUMAN PRESCRIPTION DRUG |
METFORMIN HYDROCHLORIDE |
metformin hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20191125 |
N/A |
ANDA |
ANDA212969 |
GLENMARK PHARMACEUTICALS INC., USA |
METFORMIN HYDROCHLORIDE |
1000 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-521-01) |
68462-521-05 |
68462-521 |
HUMAN PRESCRIPTION DRUG |
METFORMIN HYDROCHLORIDE |
metformin hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20191125 |
N/A |
ANDA |
ANDA212969 |
GLENMARK PHARMACEUTICALS INC., USA |
METFORMIN HYDROCHLORIDE |
1000 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-521-05) |
68462-521-90 |
68462-521 |
HUMAN PRESCRIPTION DRUG |
METFORMIN HYDROCHLORIDE |
metformin hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20191125 |
N/A |
ANDA |
ANDA212969 |
GLENMARK PHARMACEUTICALS INC., USA |
METFORMIN HYDROCHLORIDE |
1000 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-521-90) |
68462-520-10 |
68462-520 |
HUMAN PRESCRIPTION DRUG |
METFORMIN HYDROCHLORIDE |
metformin hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20191125 |
N/A |
ANDA |
ANDA212969 |
GLENMARK PHARMACEUTICALS INC., USA |
METFORMIN HYDROCHLORIDE |
500 mg/1 |
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-10) |
68462-520-05 |
68462-520 |
HUMAN PRESCRIPTION DRUG |
METFORMIN HYDROCHLORIDE |
metformin hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20191125 |
N/A |
ANDA |
ANDA212969 |
GLENMARK PHARMACEUTICALS INC., USA |
METFORMIN HYDROCHLORIDE |
500 mg/1 |
500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-05) |
68462-520-01 |
68462-520 |
HUMAN PRESCRIPTION DRUG |
METFORMIN HYDROCHLORIDE |
metformin hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20191125 |
N/A |
ANDA |
ANDA212969 |
GLENMARK PHARMACEUTICALS INC., USA |
METFORMIN HYDROCHLORIDE |
500 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68462-520-01) |