PROCHLORPERAZINE MALEATE
- Product NDC
- 42291-729
- 11-digit product format
- 422910729
- Labeler code
- 42291
- Product ID
- 42291-729_d5c98b22-4515-39fe-e053-2995a90a41f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine maleate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- AvKARE
- Application
- ANDA040268
- Marketing category
- ANDA
- Marketing start
- 2020-03-30
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 42291-729-01 | 42291072901 | 100 TABLET in 1 BOTTLE (42291-729-01) | 100 tablet | 2020-03-30 | 0000-00-00 | No | No | Current |