Acetaminophen PM
- Product NDC
- 11673-556
- 11-digit product format
- 116730556
- Labeler code
- 11673
- Product ID
- 11673-556_5f319872-d416-4db9-86c4-14b91beaf876
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Diphenhydramine HCl
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Target Corporation
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2007-12-17
- Marketing end
- 2021-08-06
- 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 |
|---|
| 11673-556-31 | 11673055631 | 1 BOTTLE, PLASTIC in 1 CARTON (11673-556-31) > 80 TABLET in 1 BOTTLE, PLASTIC | 2007-12-17 | 2021-08-06 | No | No | Current |