| NDC Code | 57664-854-18 |
|---|
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (57664-854-18) |
|---|
| Product NDC | 57664-854 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Minocycline |
|---|
| Non-Proprietary Name | Minocycline Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160129 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090217 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
|---|
| Strength | 50 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tetracycline-class Drug [EPC], Tetracyclines [CS] |
|---|