| NDC Code | 0615-7590-39 |
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| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (0615-7590-39) |
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| Product NDC | 0615-7590 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Acetaminophen Extended Release |
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| Non-Proprietary Name | Acetaminophen |
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| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20000225 |
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| End Marketing Date | 20230630 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA075077 |
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| Manufacturer | NCS HealthCare of KY, LLC dba Vangard Labs |
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| Substance Name | ACETAMINOPHEN |
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| Strength | 650 |
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| Strength Unit | mg/1 |
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