PROCHLORPERAZINE MALEATE
- Product NDC
- 50090-7147
- 11-digit product format
- 500907147
- Labeler code
- 50090
- Product ID
- 50090-7147_8b09b8d5-0219-4106-8268-94d0bdbff394
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA217478
- Marketing category
- ANDA
- Marketing start
- 2023-09-13
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 5 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-7147-0 | 50090714700 | 3 TABLET, FILM COATED in 1 BOTTLE (50090-7147-0) | 2024-04-26 | No | No | Historical |
| 50090-7147-5 | 50090714705 | 6 TABLET, FILM COATED in 1 BOTTLE (50090-7147-5) | 2024-05-01 | No | No | Historical |