Prochlorperazine Maleate
- Product NDC
- 67296-1405
- 11-digit product format
- 672961405
- Labeler code
- 67296
- Product ID
- 67296-1405_9c9f9369-3137-3cec-e053-2a95a90a8cef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA040185
- Marketing category
- ANDA
- Marketing start
- 1996-11-18
- Marketing end
- 0000-00-00
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- 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 |
|---|
| 67296-1405-5 | Prochlorperazine Maleate | 15 in 1 BOTTLE | TABLET, FILM COATED | 15 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1405 | PROCHLORPERAZINE MALEATE TABLET, FILM COATED [REDPHARM DRUG, INC.] | 3 | Legacy NDC, 1 package rows | 20200122_50d5094e-07f9-5162-e054-00144ff88e88.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 |
|---|
| 67296-1405-5 | 67296140505 | 15 TABLET, FILM COATED in 1 BOTTLE (67296-1405-5) | 1996-11-18 | 0000-00-00 | No | No | Current |