Perphenazine
- Product NDC
- 72162-2397
- 11-digit product format
- 721622397
- Labeler code
- 72162
- Product ID
- 72162-2397_3406ea16-124c-5e5c-e063-6394a90a8de6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA205973
- Marketing category
- ANDA
- Marketing start
- 2018-02-06
- Substance
- PERPHENAZINE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 72162-2397-1 | 72162239701 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2397-1) | 2024-09-30 | No | No | Historical |
| 72162-2397-2 | 72162239702 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2397-2) | 2025-04-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Perphenazine Tablets, USP | Bryant Ranch Prepack | 2025-04-30 | HUMAN PRESCRIPTION DRUG LABEL | 2 |