Perphenazine
- Product NDC
- 0603-5063
- 11-digit product format
- 006035063
- Labeler code
- 0603
- Product ID
- 0603-5063_984ac2cf-c025-44e1-b1bb-a73260473881
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Endo USA, Inc.
- Application
- ANDA040226
- Marketing category
- ANDA
- Marketing start
- 1998-12-31
- Substance
- PERPHENAZINE
- Active strength
- 16 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Perphenazine
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PERPHENAZINE | 16 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 |
|---|
| 0603-5063-21 | Perphenazine | 100 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 100 | | 19 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| PERPHENAZINE | ACTIVE INGREDIENT | FTA7XXY4EZ | PERPHENAZINE TABLET, FILM COATED [QUALITEST PHARMACEUTICALS] | 5 | |
| PERPHENAZINE | ACTIVE MOIETY | FTA7XXY4EZ | PERPHENAZINE TABLET, FILM COATED [QUALITEST PHARMACEUTICALS] | 5 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | PERPHENAZINE TABLET, FILM COATED [QUALITEST PHARMACEUTICALS] | 5 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | PERPHENAZINE TABLET, FILM COATED [QUALITEST PHARMACEUTICALS] | 5 | |
| FERROSOFERRIC OXIDE | INACTIVE INGREDIENT | XM0M87F357 | PERPHENAZINE TABLET, FILM COATED [QUALITEST PHARMACEUTICALS] | 5 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | PERPHENAZINE TABLET, FILM COATED [QUALITEST PHARMACEUTICALS] | 5 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | PERPHENAZINE TABLET, FILM COATED [QUALITEST PHARMACEUTICALS] | 5 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | PERPHENAZINE TABLET, FILM COATED [QUALITEST PHARMACEUTICALS] | 5 | |
| POLYVINYL ALCOHOL | INACTIVE INGREDIENT | 532B59J990 | PERPHENAZINE TABLET, FILM COATED [QUALITEST PHARMACEUTICALS] | 5 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | PERPHENAZINE TABLET, FILM COATED [QUALITEST PHARMACEUTICALS] | 5 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | PERPHENAZINE TABLET, FILM COATED [QUALITEST PHARMACEUTICALS] | 5 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | PERPHENAZINE TABLET, FILM COATED [QUALITEST PHARMACEUTICALS] | 5 | |
| PERPHENAZINE | ACTIVE INGREDIENT | FTA7XXY4EZ | PERPHENAZINE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| PERPHENAZINE | ACTIVE MOIETY | FTA7XXY4EZ | PERPHENAZINE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | PERPHENAZINE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | PERPHENAZINE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| FERROSOFERRIC OXIDE | INACTIVE INGREDIENT | XM0M87F357 | PERPHENAZINE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | PERPHENAZINE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | PERPHENAZINE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | PERPHENAZINE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| POLYVINYL ALCOHOL | INACTIVE INGREDIENT | 532B59J990 | PERPHENAZINE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | PERPHENAZINE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | PERPHENAZINE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | PERPHENAZINE TABLET, FILM COATED [STATE OF FLORIDA DOH CENTRAL PHARMACY] | 2 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0603-5063 | PERPHENAZINE TABLET, FILM COATED [ENDO USA, INC.] | 19 | Current NDC, Legacy NDC, 1 package rows | 20241212_5fbfe9da-26e8-4705-98f3-42acd3d7b439.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 |
|---|
| 0603-5063-21 | 00603506321 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0603-5063-21) | 1998-12-31 | 0000-00-00 | No | No | Current |