Diphenhydramine Hydrochloride
- Product NDC
- 60760-332
- Requested package NDC
- 60760-332-30
- 11-digit product format
- 607600332
- Labeler code
- 60760
- Product ID
- 60760-332_a0967588-5008-2cdf-e053-2995a90a2b42
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- St. Mary's Medical Park Pharmacy
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2020-03-11
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60760-332 | DIPHENHYDRAMINE HYDROCHLORIDE CAPSULE [ST. MARY'S MEDICAL PARK PHARMACY] | 2 | Legacy NDC | 20231219_a0968b34-280d-a644-e053-2a95a90a4c58.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60760-332-30 | 60760033230 | 30 CAPSULE in 1 BOTTLE, PLASTIC (60760-332-30) | 30 capsule | 2020-03-11 | 0000-00-00 | No | No | Current |