| NDC Code | 55111-637-10 |
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| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (55111-637-10) |
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| Product NDC | 55111-637 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Minocycline Hydrochloride |
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| Non-Proprietary Name | Minocycline Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20080123 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065436 |
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| Manufacturer | Dr. Reddy's Laboratories Limited |
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| Substance Name | MINOCYCLINE HYDROCHLORIDE |
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| Strength | 50 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Tetracycline-class Drug [EPC], Tetracyclines [CS] |
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