46708-574-30 |
46708-574 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Limited |
PRAMIPEXOLE DIHYDROCHLORIDE |
.375 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-574-30) |
46708-575-30 |
46708-575 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Limited |
PRAMIPEXOLE DIHYDROCHLORIDE |
.75 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-575-30) |
46708-576-30 |
46708-576 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Limited |
PRAMIPEXOLE DIHYDROCHLORIDE |
1.5 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-576-30) |
46708-577-30 |
46708-577 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Limited |
PRAMIPEXOLE DIHYDROCHLORIDE |
2.25 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-577-30) |
46708-578-30 |
46708-578 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Limited |
PRAMIPEXOLE DIHYDROCHLORIDE |
3 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-578-30) |
46708-579-30 |
46708-579 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Limited |
PRAMIPEXOLE DIHYDROCHLORIDE |
3.75 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-579-30) |
46708-580-30 |
46708-580 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Limited |
PRAMIPEXOLE DIHYDROCHLORIDE |
4.5 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (46708-580-30) |
62332-154-30 |
62332-154 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Inc. |
PRAMIPEXOLE DIHYDROCHLORIDE |
.375 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-154-30) |
62332-155-30 |
62332-155 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Inc. |
PRAMIPEXOLE DIHYDROCHLORIDE |
.75 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-155-30) |
62332-156-30 |
62332-156 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Inc. |
PRAMIPEXOLE DIHYDROCHLORIDE |
1.5 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-156-30) |
62332-157-30 |
62332-157 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Inc. |
PRAMIPEXOLE DIHYDROCHLORIDE |
2.25 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-157-30) |
62332-158-30 |
62332-158 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Inc. |
PRAMIPEXOLE DIHYDROCHLORIDE |
3 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-158-30) |
62332-159-30 |
62332-159 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Inc. |
PRAMIPEXOLE DIHYDROCHLORIDE |
4.5 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-159-30) |
62332-160-30 |
62332-160 |
HUMAN PRESCRIPTION DRUG |
Pramipexole Dihydrochloride |
Pramipexole Dihydrochloride |
TABLET, EXTENDED RELEASE |
ORAL |
20190103 |
N/A |
ANDA |
ANDA204518 |
Alembic Pharmaceuticals Inc. |
PRAMIPEXOLE DIHYDROCHLORIDE |
3.75 mg/1 |
30 TABLET, EXTENDED RELEASE in 1 BOTTLE (62332-160-30) |