DIPHENHYDRAMINE HYDROCHLORIDE 50mg
- Product NDC
- 73629-001
- 11-digit product format
- 736290001
- Labeler code
- 73629
- Product ID
- 73629-001_47d40d86-cbe8-fc70-e063-6394a90a2ff3
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- DIPHENHYDRAMINE HYDROCHLORIDE 50mg
- Dosage form
- CAPSULE, LIQUID FILLED
- Route
- ORAL
- Labeler
- AMZ789 LLC
- Application
- M010
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2020-09-21
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 50 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- DIPHENHYDRAMINE HYDROCHLORIDE 50mg
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| DIPHENHYDRAMINE HYDROCHLORIDE | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | TC2D6JAD40 |
| Rxcui | 1020477 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 73629-001-22 | DIPHENHYDRAMINE HYDROCHLORIDE 50mg | 220 in 1 BOTTLE | CAPSULE, LIQUID FILLED | 220 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73629-001 | DIPHENHYDRAMINE HYDROCHLORIDE 50MG CAPSULE, LIQUID FILLED [AMZ789 LLC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20241122_af0b1b08-e269-6399-e053-2a95a90ac12d.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73629-001-22 | 73629000122 | 220 CAPSULE, LIQUID FILLED in 1 BOTTLE (73629-001-22) | 2020-09-28 | 0000-00-00 | No | No | Current |