Prochlorperazine Maleate
- Product NDC
- 35356-672
- 11-digit product format
- 353560672
- Labeler code
- 35356
- Product ID
- 35356-672_d316add5-6ea9-4b80-9800-d1da6b68b6b9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prochlorperazine maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA040185
- Marketing category
- ANDA
- Marketing start
- 2012-11-05
- Marketing end
- 0000-00-00
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record