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Minocycline Hydrochloride
Minocycline Hydrochloride - 65862-558-30 - (Minocycline Hydrochloride)
Drug Information of Minocycline Hydrochloride
| Product NDC: | 65862-558 |
| Proprietary Name: | Minocycline Hydrochloride |
| 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 Minocycline Hydrochloride
| Product NDC: | 65862-558 |
| Labeler Name: | Aurobindo Pharma Limited |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA202261 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20121119 |
Package Information of Minocycline Hydrochloride
| Package NDC: | 65862-558-30 |
| Package Description: | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-558-30) |
NDC Information of Minocycline Hydrochloride
| NDC Code | 65862-558-30 |
| Proprietary Name | Minocycline Hydrochloride |
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (65862-558-30) |
| Product NDC | 65862-558 |
| 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 | 20121119 |
| Marketing Category Name | ANDA |
| Labeler Name | Aurobindo Pharma Limited |
| Substance Name | MINOCYCLINE HYDROCHLORIDE |
| Strength Number | 135 |
| Strength Unit | mg/1 |
| Pharmaceutical Classes | Tetracycline-class Drug [EPC],Tetracyclines [Chemical/Ingredient] |
