Benadryl
- Product NDC
- 21695-811
- 11-digit product format
- 216950811
- Labeler code
- 21695
- Product ID
- 21695-811_9c3fc14a-551c-4957-9074-6b27dfd4a29f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2009-01-01
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 21695-811-24 | BenadrylAllergy | 3 in 1 CARTON | TABLET, COATED | 3 | | 1 |
| 21695-811-24 | BenadrylAllergy | 8 in 1 BLISTER PACK | TABLET, COATED | 8 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-811 | BENADRYL ALLERGY (DIPHENHYDRAMINE HYDROCHLORIDE) TABLET, COATED [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 2 package rows | 20110414_9c3fc14a-551c-4957-9074-6b27dfd4a29f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-811-24 | 21695081124 | 3 in 1 CARTON | Historical |