sleep aid
- Product NDC
- 71713-100
- 11-digit product format
- 717130100
- Labeler code
- 71713
- Product ID
- 71713-100_2b5ac07f-7690-4ca4-95ee-d8369e69d104
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- THIRTY MADISON INC
- Application
- part338
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2022-04-26
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71713-100-51 | 71713010051 | 12 BLISTER PACK in 1 CARTON (71713-100-51) > 2 TABLET, FILM COATED in 1 BLISTER PACK | 12 blister pack | 2022-04-26 | 0000-00-00 | No | No | Current |