Prochlorperazine Maleate
- Product NDC
- 63187-877
- 11-digit product format
- 631870877
- Labeler code
- 63187
- Product ID
- 63187-877_ef9eb921-e5e0-484f-9c8c-056fdef111f4
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Prochlorperazine Maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA040120
- Marketing category
- ANDA
- Marketing start
- 1996-07-25
- 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 |
|---|
| 63187-877-15 | 63187087715 | 15 TABLET, FILM COATED in 1 BOTTLE (63187-877-15) | 2017-08-01 | 0000-00-00 | No | No | Current |
| 63187-877-30 | 63187087730 | 30 TABLET, FILM COATED in 1 BOTTLE (63187-877-30) | 2017-08-01 | 0000-00-00 | No | No | Current |
| 63187-877-60 | 63187087760 | 60 TABLET, FILM COATED in 1 BOTTLE (63187-877-60) | 2017-08-01 | 0000-00-00 | No | No | Current |
| 63187-877-90 | 63187087790 | 90 TABLET, FILM COATED in 1 BOTTLE (63187-877-90) | 2017-08-01 | 0000-00-00 | No | No | Current |