Prochlorperazine Maleate
- Product NDC
- 50090-1854
- 11-digit product format
- 500901854
- Labeler code
- 50090
- Product ID
- 50090-1854_24ca66aa-b507-4610-bfe0-76ed549cfefb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prochlorperazine maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA040185
- Marketing category
- ANDA
- Marketing start
- 1996-11-18
- 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1854-0 | 50090185400 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-1854-0) | 2015-06-02 | 0000-00-00 | No | No | Current |