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Solodyn
Solodyn - 99207-462-01 - (minocycline hydrochloride)
Drug Information of Solodyn
| Product NDC: | 99207-462 |
| Proprietary Name: | Solodyn |
| Non Proprietary Name: | minocycline hydrochloride |
| Active Ingredient(s): | 135 mg/1 & nbsp; minocycline hydrochloride |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET, FILM COATED, EXTENDED RELEASE |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Solodyn
| Product NDC: | 99207-462 |
| Labeler Name: | Medicis Pharmaceutical Corp. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | NDA050808 |
| Marketing Category: | NDA |
| Start Marketing Date: | 20060508 |
Package Information of Solodyn
| Package NDC: | 99207-462-01 |
| Package Description: | 20 BLISTER PACK in 1 CARTON (99207-462-01) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
NDC Information of Solodyn
| NDC Code | 99207-462-01 |
| Proprietary Name | Solodyn |
| Package Description | 20 BLISTER PACK in 1 CARTON (99207-462-01) > 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK |
| Product NDC | 99207-462 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | minocycline hydrochloride |
| Dosage Form Name | TABLET, FILM COATED, EXTENDED RELEASE |
| Route Name | ORAL |
| Start Marketing Date | 20060508 |
| Marketing Category Name | NDA |
| Labeler Name | Medicis Pharmaceutical Corp. |
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
| Strength Number | 135 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
