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Arestin
Arestin - 65976-100-01 - (Minocycline Hydrochloride)
Drug Information of Arestin
| Product NDC: | 65976-100 |
| Proprietary Name: | Arestin |
| Non Proprietary Name: | Minocycline Hydrochloride |
| Active Ingredient(s): | 1 mg/1 & nbsp; Minocycline Hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | POWDER |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Arestin
| Product NDC: | 65976-100 |
| Labeler Name: | OraPharma, Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050781 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20110321 |
Package Information of Arestin
| Package NDC: | 65976-100-01 |
| Package Description: | 1 POWDER in 1 POUCH (65976-100-01) |
NDC Information of Arestin
| NDC Code | 65976-100-01 |
| Proprietary Name | Arestin |
| Package Description | 1 POWDER in 1 POUCH (65976-100-01) |
| Product NDC | 65976-100 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Minocycline Hydrochloride |
| Dosage Form Name | POWDER |
| Route Name | ORAL |
| Start Marketing Date | 20110321 |
| Marketing Category Name | NDA |
| Labeler Name | OraPharma, Inc. |
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
| Strength Number | 1 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
