Prochlorperazine Maleate
- Product NDC
- 55289-568
- 11-digit product format
- 552890568
- Labeler code
- 55289
- Product ID
- 55289-568_7a8bd0b4-14fd-5d56-e053-2991aa0a2beb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prochlorperazine maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA040185
- Marketing category
- ANDA
- Marketing start
- 1996-11-18
- Marketing end
- 0000-00-00
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 5 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