PROCHLORPERAZINE MALEATE
- Product NDC
- 67296-2195
- 11-digit product format
- 672962195
- Labeler code
- 67296
- Product ID
- 67296-2195_4727abc5-0f6a-867f-e063-6294a90ae8ae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Redpharm Drug
- Application
- ANDA217478
- Marketing category
- ANDA
- Marketing start
- 2025-01-31
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| I1T8O1JTL6 | PROCHLORPERAZINE MALEATE | 84-02-6 | PROCHLORPERAZINE MALEATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67296-2195-1 | 67296219501 | 100 TABLET in 1 BOTTLE (67296-2195-1) | 100 tablet | 2025-01-31 | No | No | Historical |
| 67296-2195-2 | 67296219502 | 15 TABLET in 1 BOTTLE (67296-2195-2) | 15 tablet | 2025-01-31 | No | No | Historical |