| NDC Code | 0115-2122-02 |
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| Package Description | 500 TABLET, FILM COATED in 1 BOTTLE (0115-2122-02) |
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| Product NDC | 0115-2122 |
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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 | 20040322 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA065094 |
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| Manufacturer | Global Pharmaceuticals, Division of Impax Laboratories, Inc. |
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| Substance Name | DEMECLOCYCLINE HYDROCHLORIDE |
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| Strength | 300 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Tetracycline-class Antimicrobial [EPC],Tetracyclines [Chemical/Ingredient] |
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