Promethazine Hydrochloride
- Product NDC
- 50090-6216
- 11-digit product format
- 500906216
- Labeler code
- 50090
- Product ID
- 50090-6216_1c01d8a6-6054-4fb9-9cab-bfcca358a1fc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA091179
- Marketing category
- ANDA
- Marketing start
- 2022-06-22
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 12.5 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Promethazine Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PROMETHAZINE HYDROCHLORIDE | 12.5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | R61ZEH7I1I |
| Rxcui | 992438 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 50090-6216-1 | Promethazine Hydrochloride | 21 in 1 BOTTLE | TABLET | 21 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 50090-6216 | PROMETHAZINE HYDROCHLORIDE TABLET [A-S MEDICATION SOLUTIONS] | 3 | Current NDC, Legacy NDC, 1 package rows | 20231101_bf951b5b-6e38-44a9-895e-0d60c6b9d343.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 |
|---|
| 50090-6216-1 | 50090621601 | 21 TABLET in 1 BOTTLE (50090-6216-1) | 21 tablet | 2022-11-09 | 0000-00-00 | No | No | Current |