Home
>
National Drug Code (NDC)
>
Minocin
Minocin - 16781-400-96 - (MINOCYCLINE HYDROCHLORIDE)
Drug Information of Minocin
| Product NDC: | 16781-400 |
| Proprietary Name: | Minocin |
| Non Proprietary Name: | MINOCYCLINE HYDROCHLORIDE |
| Active Ingredient(s): | 50 mg/1 & nbsp; MINOCYCLINE HYDROCHLORIDE |
| Administration Route(s): | ORAL |
| Dosage Form(s): | CAPSULE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Minocin
| Product NDC: | 16781-400 |
| Labeler Name: | Onset Dermatologics, LLC |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050649 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20130507 |
Package Information of Minocin
| Package NDC: | 16781-400-96 |
| Package Description: | 100 CAPSULE in 1 BOTTLE (16781-400-96) |
NDC Information of Minocin
| NDC Code | 16781-400-96 |
| Proprietary Name | Minocin |
| Package Description | 100 CAPSULE in 1 BOTTLE (16781-400-96) |
| Product NDC | 16781-400 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | MINOCYCLINE HYDROCHLORIDE |
| Dosage Form Name | CAPSULE |
| Route Name | ORAL |
| Start Marketing Date | 20130507 |
| Marketing Category Name | NDA |
| Labeler Name | Onset Dermatologics, LLC |
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
| Strength Number | 50 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
