Perphenazine
- Product NDC
- 63629-2251
- 11-digit product format
- 636292251
- Labeler code
- 63629
- Product ID
- 63629-2251_91ba4d24-907f-40b0-b5a2-1e3d5ebee04e
- 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 |
|---|
| 63629-2251-1 | Perphenazine | 500 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 500 | | 103 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-2251 | PERPHENAZINE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 103 | Current NDC, Legacy NDC, 1 package rows | 20230306_59b1a63e-6cba-4102-a5e8-83dca540341d.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 |
|---|
| 63629-2251-1 | 63629225101 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63629-2251-1) | 1998-12-31 | 0000-00-00 | No | No | Current |