Plus Pharma Extra Strength Acetaminophen PM
- Product NDC
- 51645-709
- 11-digit product format
- 516450709
- Labeler code
- 51645
- Product ID
- 51645-709_994fb1ab-d6e7-610f-e053-2a95a90a25c3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen,Diphenhydramine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Gemini Pharmaceuticals, Inc. dba Plus Pharma
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2006-03-27
- Marketing end
- 2021-06-30
- Substance
- ACETAMINOPHEN; DIPHENHYDRAMINE 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51645-709-05 | 51645070905 | 50 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51645-709-05) | 2006-03-27 | 2021-06-30 | No | No | Current |