acetaminophen pm
- Product NDC
- 30142-530
- 11-digit product format
- 301420530
- Labeler code
- 30142
- Product ID
- 30142-530_49babdf6-2312-41ab-ac82-2d65f3c45afb
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Diphenhydramine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Kroger Company
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2015-12-23
- Marketing end
- 2023-03-31
- Substance
- ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 500 mg/1; mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 30142-530-71 | 30142053071 | 1 BOTTLE in 1 CARTON (30142-530-71) > 50 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2015-12-23 | 2023-03-31 | No | No | Current |
| 30142-530-78 | 30142053078 | 1 BOTTLE in 1 CARTON (30142-530-78) > 100 TABLET, FILM COATED in 1 BOTTLE | 1 bottle | 2015-12-23 | 2023-03-31 | No | No | Current |
| 30142-530-82 | 30142053082 | 2 BOTTLE in 1 CARTON (30142-530-82) > 100 TABLET, FILM COATED in 1 BOTTLE | 2 bottle | 2015-12-23 | 2023-03-31 | No | No | Current |