47335-306-18 |
47335-306 |
HUMAN PRESCRIPTION DRUG |
Metformin Hydrochloride |
Metformin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20180522 |
N/A |
ANDA |
ANDA202917 |
Sun Pharmaceutical Industries, Inc. |
METFORMIN HYDROCHLORIDE |
1000 mg/1 |
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-18) |
47335-306-81 |
47335-306 |
HUMAN PRESCRIPTION DRUG |
Metformin Hydrochloride |
Metformin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20190722 |
N/A |
ANDA |
ANDA202917 |
Sun Pharmaceutical Industries, Inc. |
METFORMIN HYDROCHLORIDE |
1000 mg/1 |
90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-81) |
47335-305-88 |
47335-305 |
HUMAN PRESCRIPTION DRUG |
Metformin Hydrochloride |
Metformin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20180522 |
N/A |
ANDA |
ANDA202917 |
Sun Pharmaceutical Industries, Inc. |
METFORMIN HYDROCHLORIDE |
500 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-305-88) |
47335-305-83 |
47335-305 |
HUMAN PRESCRIPTION DRUG |
Metformin Hydrochloride |
Metformin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20180522 |
N/A |
ANDA |
ANDA202917 |
Sun Pharmaceutical Industries, Inc. |
METFORMIN HYDROCHLORIDE |
500 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-305-83) |
47335-305-18 |
47335-305 |
HUMAN PRESCRIPTION DRUG |
Metformin Hydrochloride |
Metformin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20180522 |
N/A |
ANDA |
ANDA202917 |
Sun Pharmaceutical Industries, Inc. |
METFORMIN HYDROCHLORIDE |
500 mg/1 |
1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-305-18) |
47335-306-83 |
47335-306 |
HUMAN PRESCRIPTION DRUG |
Metformin Hydrochloride |
Metformin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20180522 |
N/A |
ANDA |
ANDA202917 |
Sun Pharmaceutical Industries, Inc. |
METFORMIN HYDROCHLORIDE |
1000 mg/1 |
30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-83) |
47335-306-88 |
47335-306 |
HUMAN PRESCRIPTION DRUG |
Metformin Hydrochloride |
Metformin Hydrochloride |
TABLET, FILM COATED, EXTENDED RELEASE |
ORAL |
20180522 |
N/A |
ANDA |
ANDA202917 |
Sun Pharmaceutical Industries, Inc. |
METFORMIN HYDROCHLORIDE |
1000 mg/1 |
100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (47335-306-88) |