| NDC Code | 57664-853-85 |
|---|
| Package Description | 50 CAPSULE in 1 BOTTLE (57664-853-85) |
|---|
| Product NDC | 57664-853 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Minocycline Hydrochloride |
|---|
| Non-Proprietary Name | Minocycline Hydrochloride |
|---|
| Dosage Form | CAPSULE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20130513 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090867 |
|---|
| Manufacturer | Sun Pharmaceutical Industries, Inc. |
|---|
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
|---|
| Strength | 100 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Decreased Prothrombin Activity [PE], Tetracycline-class Drug [EPC], Tetracyclines [CS] |
|---|