Perphenazine
- Product NDC
- 72162-1163
- 11-digit product format
- 721621163
- Labeler code
- 72162
- Product ID
- 72162-1163_baac14ec-3afe-4921-a123-5801a1ec6b63
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040226
- Marketing category
- ANDA
- Marketing start
- 1998-12-31
- 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Perphenazine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PERPHENAZINE | 4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | FTA7XXY4EZ |
| Rxcui | 198077 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1163-1 | Perphenazine | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1163 | PERPHENAZINE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20230913_9ad131c1-0620-4d3c-9734-bcffd98430e2.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1163-1 | 72162116301 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72162-1163-1) | 2023-09-12 | No | No | Current |