Promethazine Hydrochloride
- Product NDC
- 67296-0086
- 11-digit product format
- 672960086
- Labeler code
- 67296
- Product ID
- 67296-0086_d5fbea2f-f34c-900f-e053-2995a90a3887
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Promethazine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA083426
- Marketing category
- ANDA
- Marketing start
- 1973-09-19
- Marketing end
- 0000-00-00
- Substance
- PROMETHAZINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 67296-0086-1 | Promethazine Hydrochloride | 15 in 1 BOTTLE | TABLET | 15 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0086 | PROMETHAZINE HYDROCHLORIDE TABLET [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 1 package rows | 20220120_4e8ebc4a-9a13-749a-e054-00144ff8d46c.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 |
|---|
| 67296-0086-1 | 67296008601 | 15 TABLET in 1 BOTTLE (67296-0086-1) | 15 tablet | 1973-09-19 | 0000-00-00 | No | No | Current |