Prochlorperazine Maleate
- Product NDC
- 67296-0577
- 11-digit product format
- 672960577
- Labeler code
- 67296
- Product ID
- 67296-0577_9c9ae269-c660-4cd8-e053-2995a90ab98e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA040120
- Marketing category
- ANDA
- Marketing start
- 1996-07-25
- 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 |
|---|
| 67296-0577-1 | Prochlorperazine Maleate | 15 in 1 BOTTLE | TABLET, FILM COATED | 15 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0577 | PROCHLORPERAZINE MALEATE TABLET, FILM COATED [REDPHARM DRUG, INC.] | 4 | Legacy NDC, 1 package rows | 20200121_4d9cd6b2-329f-539d-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 |
|---|
| 67296-0577-1 | 67296057701 | 15 TABLET, FILM COATED in 1 BOTTLE (67296-0577-1) | 1996-07-25 | 0000-00-00 | No | No | Current |