Allergy
- Product NDC
- 55319-932
- Requested package NDC
- 55319-932-22
- 11-digit product format
- 553190932
- Labeler code
- 55319
- Product ID
- 55319-932_d260aaee-90be-45d9-ad5e-a98e743256e9
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine HCl
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Family Dollar Services Inc
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 1990-03-02
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 25 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
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 55319-932 | 55319-932-22 | D | Discontinued by firm | 2026-10-12 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Dashboard NDC Coverage#
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 55319-932-22 | 55319093222 | 4 BLISTER PACK in 1 CARTON (55319-932-22) > 12 TABLET, FILM COATED in 1 BLISTER PACK | 4 blister pack | 1990-03-02 | 0000-00-00 | No | No | Current |