Pain Reliever PM
- Product NDC
- 59726-032
- Requested package NDC
- 59726-032-50
- 11-digit product format
- 597260032
- Labeler code
- 59726
- Product ID
- 59726-032_0c012085-b9e1-4b90-8c4a-421e2a4e67c6
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Acetaminophen Diphenhydramine HCI
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- P & L Development, LLC
- Application
- part343
- Marketing category
- OTC MONOGRAPH NOT FINAL
- Marketing start
- 2017-12-31
- Marketing end
- 0000-00-00
- Substance
- ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 500 mg/1; mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59726-032 | PAIN RELIEVER PM EXTRA STRENGTH (ACETAMINOPHEN DIPHENHYDRAMINE HCI) TABLET, COATED [P & L DEVELOPMENT, LLC] | 3 | Legacy NDC | 20230303_9ec9e54c-0616-415c-9ecd-ebfa04acebd4.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59726-032-50 | 59726003250 | 500 TABLET, COATED in 1 BOTTLE, PLASTIC (59726-032-50) | 2017-12-31 | 0000-00-00 | No | No | Current |