Perphenazine
- Product NDC
- 72162-2399
- 11-digit product format
- 721622399
- Labeler code
- 72162
- Product ID
- 72162-2399_883d9699-3692-445e-bc6b-1d30e547baa3
- 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
- 16 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Perphenazine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PERPHENAZINE | 16 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | FTA7XXY4EZ |
| Rxcui | 198075 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2399-1 | Perphenazine | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 3 |
| 72162-2399-2 | Perphenazine | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2399 | PERPHENAZINE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 2 | Current NDC, 2 package rows | 20250502_41758282-6848-4a47-bbf3-89edc270f7b3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-2399-1 | 72162239901 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2399-1) | 2024-09-30 | No | No | Historical |
| 72162-2399-2 | 72162239902 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2399-2) | 2025-04-30 | No | No | Historical |