Perphenazine
- Product NDC
- 0591-4101
- 11-digit product format
- 005914101
- Labeler code
- 0591
- Product ID
- 0591-4101_ac53b4c3-a05c-4ffc-a9ee-82bc1664fbc2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA207582
- Marketing category
- ANDA
- Marketing start
- 2017-05-30
- Substance
- PERPHENAZINE
- Active strength
- 2 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 | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | FTA7XXY4EZ |
| Rxcui | 198075, 198076, 198077, 198078 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0591-4101-01 | Perphenazine | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 13 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0591-4101 | PERPHENAZINE TABLET, FILM COATED [ACTAVIS PHARMA, INC.] | 13 | Current NDC, Legacy NDC, 1 package rows | 20250507_bb1a3d20-1f93-48a1-9e27-4712a8561757.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0591-4101-01 | 00591410101 | 100 TABLET, FILM COATED in 1 BOTTLE (0591-4101-01) | 2017-05-30 | 0000-00-00 | No | No | Current |