Acetaminophen PM
- Product NDC
- 37012-771
- 11-digit product format
- 370120771
- Labeler code
- 37012
- Product ID
- 37012-771_945a7858-7940-ae39-e053-2995a90aa72e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen and Diphenhydramine Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Shopko Stores Operating Co., LLC
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2017-11-01
- Marketing end
- 2021-04-30
- 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 |
|---|
| 37012-771-01 | 37012077101 | 1 BOTTLE, PLASTIC in 1 CARTON (37012-771-01) > 20 TABLET, COATED in 1 BOTTLE, PLASTIC | 2017-11-01 | 2021-02-28 | No | No | Current |
| 37012-771-03 | 37012077103 | 1 BOTTLE, PLASTIC in 1 CARTON (37012-771-03) > 80 TABLET, COATED in 1 BOTTLE, PLASTIC | 2017-11-01 | 2021-04-30 | No | No | Current |