| NDC Code | 51645-709-05 |
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| Package Description | 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51645-709-05) |
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| Product NDC | 51645-709 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Plus Pharma Extra Strength Acetaminophen Pm |
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| Non-Proprietary Name | Acetaminophen,diphenhydramine Hcl |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20060327 |
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| End Marketing Date | 20210630 |
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| Marketing Category Name | OTC MONOGRAPH NOT FINAL |
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| Application Number | part343 |
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| Manufacturer | Gemini Pharmaceuticals, Inc. dba Plus Pharma |
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| Substance Name | ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE |
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| Strength | 500; 25 |
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| Strength Unit | mg/1; mg/1 |
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