Perphenazine
- Product NDC
- 63629-7252
- 11-digit product format
- 636297252
- Labeler code
- 63629
- Product ID
- 63629-7252_4e72fecf-2be9-49dd-8a3c-12b3e5209200
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040226
- Marketing category
- ANDA
- Marketing start
- 1998-12-31
- Marketing end
- 0000-00-00
- Substance
- PERPHENAZINE
- Active strength
- 8 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| FTA7XXY4EZ | PERPHENAZINE | 58-39-9 | PERPHENAZINE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7252-1 | 63629725201 | 30 TABLET, FILM COATED in 1 BOTTLE (63629-7252-1) | 2021-12-22 | 0000-00-00 | No | No | Current |