Product NDC: | 14290-570 |
Proprietary Name: | Minocin Kit |
Non Proprietary Name: | minocycline hydrochloride |
Active Ingredient(s): | 100 mg/1 & nbsp; minocycline hydrochloride |
Administration Route(s): | ORAL |
Dosage Form(s): | CAPSULE, COATED PELLETS |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 14290-570 |
Labeler Name: | Triax Pharmaceuticals, LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA050649 |
Marketing Category: | NDA |
Start Marketing Date: | 20070901 |
Package NDC: | 14290-570-93 |
Package Description: | 1 BOTTLE in 1 CARTON (14290-570-93) > 5 CAPSULE, COATED PELLETS in 1 BOTTLE |
NDC Code | 14290-570-93 |
Proprietary Name | Minocin Kit |
Package Description | 1 BOTTLE in 1 CARTON (14290-570-93) > 5 CAPSULE, COATED PELLETS in 1 BOTTLE |
Product NDC | 14290-570 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | minocycline hydrochloride |
Dosage Form Name | CAPSULE, COATED PELLETS |
Route Name | ORAL |
Start Marketing Date | 20070901 |
Marketing Category Name | NDA |
Labeler Name | Triax Pharmaceuticals, LLC |
Substance Name | MINOCYCLINE HYDROCHLORIDE |
Strength Number | 100 |
Strength Unit | mg/1 |
Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |