Perphenazine
- Product NDC
- 53808-1124
- 11-digit product format
- 538081124
- Labeler code
- 53808
- Product ID
- 53808-1124_c8e7481c-7e5a-4ea6-898a-dbb92d2674eb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- DOH CENTRAL PHARMACY
- Application
- ANDA205973
- Marketing category
- ANDA
- Marketing start
- 2018-06-01
- Marketing end
- 0000-00-00
- Substance
- PERPHENAZINE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
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 |
|---|
| 53808-1124-1 | Perphenazine | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 53808-1124 | PERPHENAZINE TABLET, FILM COATED [DOH CENTRAL PHARMACY] | 1 | Legacy NDC, 1 package rows | 20190125_ef44f1e9-0826-4670-9b98-8bdd2189b3c7.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 |
|---|
| 53808-1124-1 | 53808112401 | 30 TABLET, FILM COATED in 1 BLISTER PACK (53808-1124-1) | 2018-06-01 | 0000-00-00 | No | No | Current |