Perphenazine
- Product NDC
- 70518-1125
- 11-digit product format
- 705181125
- Labeler code
- 70518
- Product ID
- 70518-1125_485a8941-0492-10ff-e063-6394a90a6a85
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205973
- Marketing category
- ANDA
- Marketing start
- 2018-04-19
- Substance
- PERPHENAZINE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Perphenazine
- Listing expiration
- 2027-12-31
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 |
|---|
| 70518-1125-0 | Perphenazine | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 14 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-1125 | PERPHENAZINE TABLET, FILM COATED [REMEDYREPACK INC.] | 12 | Current NDC, Legacy NDC, 1 package rows | 20250507_1a216d3f-12b0-44c2-b7d3-109fee45978d.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 |
|---|
| 70518-1125-0 | 70518112500 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1125-0) | 2018-04-19 | 0000-00-00 | No | No | Current |