Prochlorperazine Maleate
- Product NDC
- 51079-541
- 11-digit product format
- 510790541
- Labeler code
- 51079
- Product ID
- 51079-541_9b049a10-75a7-e1ef-e053-2a95a90aaf77
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prochlorperazine maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Institutional Inc.
- Application
- ANDA040185
- Marketing category
- ANDA
- Marketing start
- 1997-04-15
- Marketing end
- 2020-01-31
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record