PROCHLORPERAZINE MALEATE
- Product NDC
- 71335-2386
- 11-digit product format
- 713352386
- Labeler code
- 71335
- Product ID
- 71335-2386_351c034c-50e3-1546-e063-6394a90a7f26
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA217478
- Marketing category
- ANDA
- Marketing start
- 2023-09-13
- 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 | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2386-1 | 71335238601 | 10 TABLET, FILM COATED in 1 BOTTLE (71335-2386-1) | 2024-05-29 | No | No | Historical |
| 71335-2386-2 | 71335238602 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-2386-2) | 2024-05-29 | No | No | Historical |
| 71335-2386-3 | 71335238603 | 20 TABLET, FILM COATED in 1 BOTTLE (71335-2386-3) | 2024-05-29 | No | No | Historical |
| 71335-2386-4 | 71335238604 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-2386-4) | 2024-05-29 | No | No | Historical |
| 71335-2386-5 | 71335238605 | 4 TABLET, FILM COATED in 1 BOTTLE (71335-2386-5) | 2024-05-29 | No | No | Historical |
| 71335-2386-6 | 71335238606 | 5 TABLET, FILM COATED in 1 BOTTLE (71335-2386-6) | 2024-05-29 | No | No | Historical |
| 71335-2386-7 | 71335238607 | 100 TABLET, FILM COATED in 1 BOTTLE (71335-2386-7) | 2024-05-29 | No | No | Historical |
| 71335-2386-8 | 71335238608 | 6 TABLET, FILM COATED in 1 BOTTLE (71335-2386-8) | 2024-05-29 | No | No | Historical |