Perphenazine
- Product NDC
- 53808-0938
- 11-digit product format
- 538080938
- Labeler code
- 53808
- Product ID
- 53808-0938_6a4cea14-a6b0-4d95-a7cf-b14a6bdab0ce
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA040226
- Marketing category
- ANDA
- Marketing start
- 2014-01-01
- Marketing end
- 0000-00-00
- Substance
- PERPHENAZINE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| FTA7XXY4EZ | PERPHENAZINE | 58-39-9 | PERPHENAZINE |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| PERPHENAZINE TABLETS, USP | State of Florida DOH Central Pharmacy | 2015-01-18 | HUMAN PRESCRIPTION DRUG LABEL | 2 |