Perphenazine
- Product NDC
- 0781-8047
- 11-digit product format
- 007818047
- Labeler code
- 0781
- Product ID
- 0781-8047_9e348a80-ecb9-409b-91e7-3a48423314ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sandoz Inc
- Application
- ANDA089685
- Marketing category
- ANDA
- Marketing start
- 1988-12-08
- Marketing end
- 2027-03-21
- Substance
- PERPHENAZINE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Perphenazine
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PERPHENAZINE | 4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | FTA7XXY4EZ |
| Rxcui | 198075, 198076, 198077, 198078 |
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0781-8047-01 | Perphenazine | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0781-8047 | PERPHENAZINE TABLET, FILM COATED [SANDOZ INC] | 4 | Current NDC, Legacy NDC, 1 package rows | 20240322_fc32500c-cc42-4f85-9cee-88f983fcbc16.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 |
|---|
| 0781-8047-01 | 00781804701 | 100 TABLET, FILM COATED in 1 BOTTLE (0781-8047-01) | 2018-08-28 | 2027-03-21 | No | No | Current |