pain relief PM
- Product NDC
- 41250-756
- 11-digit product format
- 412500756
- Labeler code
- 41250
- Product ID
- 41250-756_1773f9a8-9968-47ba-9544-1f203f2a7534
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen, Diphenhydramine HCl
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Meijer Distribution Inc
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2020-08-18
- Marketing end
- 0000-00-00
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 41250-756 | PAIN RELIEF PM (ACETAMINOPHEN, DIPHENHYDRAMINE HCL) TABLET, COATED [MEIJER DISTRIBUTION INC] | 6 | Legacy NDC | 20240619_4f33df5e-de85-41bf-9126-c0ee679d7ef2.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 41250-756-31 | 41250075631 | 80 TABLET, COATED in 1 BOTTLE, PLASTIC (41250-756-31) | 2020-08-18 | 0000-00-00 | No | No | Current |