Prochlorperazine Maleate
- Product NDC
- 67296-0570
- 11-digit product format
- 672960570
- Labeler code
- 67296
- Product ID
- 67296-0570_40e45126-37f0-1c38-e054-00144ff8d46c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET
- 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
- 10 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- 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 |
|---|
| 67296-0570-2 | Prochlorperazine Maleate | 15 in 1 BOTTLE | TABLET | 15 | | 2 |
| 67296-0570-3 | Prochlorperazine Maleate | 10 in 1 BOTTLE | TABLET | 10 | | 2 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-0570 | PROCHLORPERAZINE MALEATE TABLET [REDPHARM DRUG, INC.] | 2 | Legacy NDC, 2 package rows | 20161110_40e45126-37ef-1c38-e054-00144ff8d46c.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 67296-0570-2 | 67296057002 | 15 in 1 BOTTLE | Historical |
| 67296-0570-3 | 67296057003 | 10 in 1 BOTTLE | Historical |