Prochlorperazine Maleate
- Product NDC
- 61919-653
- 11-digit product format
- 619190653
- Labeler code
- 61919
- Product ID
- 61919-653_92d93b94-e4bc-f3d5-e053-2995a90ac6c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA040185
- Marketing category
- ANDA
- Marketing start
- 2019-04-19
- 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 |
|---|
| 61919-653-30 | 61919065330 | 30 TABLET, FILM COATED in 1 BOTTLE (61919-653-30) | 2019-09-18 | 0000-00-00 | No | No | Current |