PROCHLORPERAZINE MALEATE
- Product NDC
- 61919-908
- 11-digit product format
- 619190908
- Labeler code
- 61919
- Product ID
- 61919-908_92d93b94-e4bc-f3d5-e053-2995a90ac6c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- PROCHLORPERAZINE MALEATE
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Direct_Rx
- Application
- ANDA040268
- Marketing category
- ANDA
- Marketing start
- 2017-01-01
- 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 |
|---|
| 61919-908-30 | 61919090830 | 30 TABLET, FILM COATED in 1 BOTTLE (61919-908-30) | 2017-11-01 | 0000-00-00 | No | No | Current |