Perphenazine
- Product NDC
- 52959-940
- 11-digit product format
- 529590940
- Labeler code
- 52959
- Product ID
- 52959-940_5db5cff3-00dc-4766-abff-66800c268e61
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- perphenazine
- Dosage form
- TABLET, SUGAR COATED
- Route
- ORAL
- Labeler
- H.J. Harkins Company, Inc.
- Application
- ANDA040226
- Marketing category
- ANDA
- Marketing start
- 1998-12-31
- 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 |
|---|
| 52959-940-60 | Perphenazine | 60 in 1 BOTTLE, PLASTIC | TABLET, SUGAR COATED | 60 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 52959-940 | PERPHENAZINE TABLET, SUGAR COATED [H.J. HARKINS COMPANY, INC.] | 2 | Legacy NDC, 1 package rows | 20111221_dd02a11f-6ea6-42e7-b168-bf2b9f4d54ae.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 52959-940-60 | 52959094060 | 60 in 1 BOTTLE, PLASTIC | Historical |