| NDC Code | 47335-669-13 |
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| Package Description | 500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (47335-669-13) |
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| Product NDC | 47335-669 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Diltiazem Hydrochloride |
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| Non-Proprietary Name | Diltiazem Hydrochloride |
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| Dosage Form | CAPSULE, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20101115 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA090421 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | DILTIAZEM HYDROCHLORIDE |
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| Strength | 120 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A4 Inhibitors [MoA] |
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