Pressure Plus Pain PE
- Product NDC
- 50804-003
- 11-digit product format
- 508040003
- Labeler code
- 50804
- Product ID
- 50804-003_7e44b298-71c7-ec26-e053-2a91aa0a2fc6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- ACETAMINOPHEN and PHENYLEPHRINE HYDROCHLORIDE
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- GoodSense
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2011-04-01
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; PHENYLEPHRINE HYDROCHLORIDE
- Active strength
- 325 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record