| NDC Code | 53489-281-10 |
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| Package Description | 1000 TABLET in 1 BOTTLE, PLASTIC (53489-281-10) |
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| Product NDC | 53489-281 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Ergoloid Mesylates |
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| Non-Proprietary Name | Dihydroergocornine Mesylate, Dihydroergocristine Mesylate, Dihydro-.alpha.-ergocryptine Mesylate, And Dihydro-.beta.-ergocryptine Mesylate |
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| Dosage Form | TABLET |
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| Usage | ORAL |
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| Start Marketing Date | 19911031 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA081113 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | DIHYDRO-.ALPHA.-ERGOCRYPTINE MESYLATE; DIHYDRO-.BETA.-ERGOCRYPTINE MESYLATE; DIHYDROERGOCORNINE MESYLATE; DIHYDROERGOCRISTINE MESYLATE |
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| Strength | .222; .111; .333; .333 |
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| Strength Unit | mg/1; mg/1; mg/1; mg/1 |
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