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- Product NDC
- 51645-269
- 11-digit product format
- 516450269
- Labeler code
- 51645
- Product ID
- 51645-269_994f716f-25e8-7007-e053-2995a90a308e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN, PHENYLEPHRINE HYDROCHLORIDE
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Gemini Pharmaceuticals, Inc.
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2010-07-05
- Marketing end
- 2019-12-31
- Substance
- ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 500 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record