| NDC Code | 10135-625-01 |
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| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (10135-625-01) |
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| Product NDC | 10135-625 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Demeclocycline Hydrochloride |
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| Non-Proprietary Name | Demeclocycline Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20160701 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065447 |
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| Manufacturer | Marlex Pharmaceuticals Inc |
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| Substance Name | DEMECLOCYCLINE HYDROCHLORIDE |
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| Strength | 150 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Tetracycline-class Antimicrobial [EPC],Tetracyclines [CS] |
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