Prochlorperazine Maleate
- Product NDC
- 50090-0111
- 11-digit product format
- 500900111
- Labeler code
- 50090
- Product ID
- 50090-0111_6d4306f3-e993-4c8b-af2a-eb282f48604e
- 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
- 5 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0111-0 | 50090011100 | 10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-0111-0) | 2014-11-28 | 0000-00-00 | No | No | Current |