Prochlorperazine Maleate
- Product NDC
- 42708-048
- 11-digit product format
- 427080048
- Labeler code
- 42708
- Product ID
- 42708-048_7ca4d17a-d9b7-4ea9-8fc6-6e4086fa0890
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- QPharma Inc
- Application
- ANDA040120
- Marketing category
- ANDA
- Marketing start
- 1996-07-25
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#