Perphenazine
- Product NDC
- 53808-0395
- 11-digit product format
- 538080395
- Labeler code
- 53808
- Product ID
- 53808-0395_533b9303-6097-4eee-a802-d7623461b82a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- perphenazine
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- State of Florida DOH Central Pharmacy
- Application
- ANDA040226
- Marketing category
- ANDA
- Marketing start
- 2009-07-01
- Marketing end
- 0000-00-00
- Substance
- PERPHENAZINE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 | 2010-05-31 | HUMAN PRESCRIPTION DRUG LABEL | 1 |