Perphenazine
- Product NDC
- 0378-5351
- 11-digit product format
- 003785351
- Labeler code
- 0378
- Product ID
- 0378-5351_c59fcb6a-2373-4bd0-b31f-b30bd26e7089
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Mylan Pharmaceuticals Inc.
- Application
- ANDA206691
- Marketing category
- ANDA
- Marketing start
- 2017-08-18
- Marketing end
- 2022-02-28
- Substance
- PERPHENAZINE
- Active strength
- 4 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0378-5351-01 | 00378535101 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-5351-01) | 2017-08-18 | 0000-00-00 | No | No | Current |