| NDC Code | 0115-1245-08 |
|---|
| Package Description | 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0115-1245-08) |
|---|
| Product NDC | 0115-1245 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Minocycline Hydrochloride |
|---|
| Non-Proprietary Name | Minocycline Hydrochloride |
|---|
| Dosage Form | TABLET, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20090203 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA090024 |
|---|
| Manufacturer | Global Pharmaceuticals, Division of Impax Laboratories Inc. |
|---|
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
|---|
| Strength | 45 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
|---|