Diphenhydramine Hydrochloride 25mg
- Product NDC
- 70692-111
- 11-digit product format
- 706920111
- Labeler code
- 70692
- Product ID
- 70692-111_b43d643e-eb34-b295-e053-2995a90a7b6f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine hydrochloride 25mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Strive Pharmaceuticals Inc
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2018-12-20
- 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
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70692-111-01 | Diphenhydramine Hydrochloride 25mg | 100 in 1 PACKAGE | TABLET | 100 | | 3 |
| 70692-111-41 | Diphenhydramine Hydrochloride 25mg | 4 in 1 PACKAGE | TABLET | 4 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70692-111 | DIPHENHYDRAMINE HYDROCHLORIDE 25MG TABLET [STRIVE PHARMACEUTICALS INC] | 3 | Legacy NDC, 2 package rows | 20201117_91e5bd4a-b981-5b26-e053-2a95a90af9fe.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70692-111-01 | 70692011101 | 100 TABLET in 1 PACKAGE (70692-111-01) | 100 tablet | 2019-01-29 | 0000-00-00 | No | No | Current |
| 70692-111-41 | 70692011141 | 4 TABLET in 1 PACKAGE (70692-111-41) | 4 tablet | 2018-12-20 | 0000-00-00 | No | No | Current |