Perphenazine
- Product NDC
- 52536-170
- 11-digit product format
- 525360170
- Labeler code
- 52536
- Product ID
- 52536-170_325b0584-e6f3-f087-e063-6394a90a64c5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Wilshire Pharmaceuticals, Inc.
- 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, 198076, 198077, 198078 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 52536-170-01 | Perphenazine | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52536-170 | PERPHENAZINE TABLET, FILM COATED [WILSHIRE PHARMACEUTICALS, INC.] | 5 | Current NDC, Legacy NDC, 1 package rows | 20250410_5e455842-4892-4795-8c9b-4109a8f30783.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 |
|---|
| 52536-170-01 | 52536017001 | 100 TABLET, FILM COATED in 1 BOTTLE (52536-170-01) | 2018-02-06 | 0000-00-00 | No | No | Current |