Perphenazine
- Product NDC
- 0904-6601
- 11-digit product format
- 009046601
- Labeler code
- 0904
- Product ID
- 0904-6601_d6aac7df-10a5-4fe2-ad3a-882af0077f16
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA040226
- Marketing category
- ANDA
- Marketing start
- 1998-12-31
- Substance
- PERPHENAZINE
- Active strength
- 8 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 | 8 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | FTA7XXY4EZ |
| Rxcui | 198076, 198077, 198078 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0904-6601-61 | Perphenazine | 100 in 1 CARTON | TABLET, FILM COATED | 100 | | 11 |
| 0904-6601-61 | Perphenazine | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 11 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-6601 | PERPHENAZINE TABLET, FILM COATED [MAJOR PHARMACEUTICALS] | 11 | Current NDC, Legacy NDC, 2 package rows | 20250424_0dc77ea9-32ee-4b6d-b69d-8c712bcf5fe4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6601-61 | 00904660161 | 100 BLISTER PACK in 1 CARTON (0904-6601-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK | 100 blister pack | 1998-12-31 | 0000-00-00 | No | No | Current |