| NDC Code | 16714-107-01 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (16714-107-01) |
|---|
| Product NDC | 16714-107 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Minocycline Hydrochloride |
|---|
| Non-Proprietary Name | Minocycline Hydrochloride |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20160613 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202261 |
|---|
| Manufacturer | NorthStar Rx LLC |
|---|
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
|---|
| Strength | 105 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Tetracycline-class Drug [EPC], Tetracyclines [CS] |
|---|