Perphenazine
- Product NDC
- 21695-415
- 11-digit product format
- 216950415
- Labeler code
- 21695
- Product ID
- 21695-415_2d821387-4b4f-4fe3-825e-750f49755baf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Application
- ANDA089685
- Marketing category
- ANDA
- Marketing start
- 2010-04-07
- Marketing end
- 0000-00-00
- Substance
- PERPHENAZINE
- Active strength
- 8 mg/1
- Pharmacologic classes
- Phenothiazine [EPC],Phenothiazines [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 21695-415-60 | Perphenazine | 60 in 1 BLISTER PACK | TABLET, FILM COATED | 60 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-415 | PERPHENAZINE TABLET, FILM COATED [REBEL DISTRIBUTORS CORP] | 1 | Legacy NDC, 1 package rows | 20110104_2d821387-4b4f-4fe3-825e-750f49755baf.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-415-60 | 21695041560 | 60 in 1 BLISTER PACK | Historical |