Prochlorperazine Maleate
- Product NDC
- 0378-5105
- 11-digit product format
- 003785105
- Labeler code
- 0378
- Product ID
- 0378-5105_86370b37-2a3d-4231-92a8-640b467db17d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- prochlorperazine maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA040185
- Marketing category
- ANDA
- Marketing start
- 1996-11-18
- Marketing end
- 2030-01-31
- Substance
- PROCHLORPERAZINE MALEATE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0378-5105-01 | 00378510501 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5105-01) | 1996-11-18 | 0000-00-00 | No | No | Current |