Perphenazine
- Product NDC
- 68084-602
- 11-digit product format
- 680840602
- Labeler code
- 68084
- Product ID
- 68084-602_43e1a84c-eb82-4f4e-e063-6394a90a2c01
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- American Health Packaging
- Application
- ANDA040226
- Marketing category
- ANDA
- Marketing start
- 2012-08-14
- Substance
- PERPHENAZINE
- Active strength
- 4 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 | 4 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | FTA7XXY4EZ |
| Rxcui | 198077, 198078 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68084-602-01 | Perphenazine | 100 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 100 | | 14 |
| 68084-602-11 | Perphenazine | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 14 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| PERPHENAZINE | ACTIVE INGREDIENT | FTA7XXY4EZ | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 5 | |
| PERPHENAZINE | ACTIVE MOIETY | FTA7XXY4EZ | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 5 | |
| CELLULOSE, MICROCRYSTALLINE | INACTIVE INGREDIENT | OP1R32D61U | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 5 | |
| FERRIC OXIDE YELLOW | INACTIVE INGREDIENT | EX438O2MRT | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 5 | |
| FERROSOFERRIC OXIDE | INACTIVE INGREDIENT | XM0M87F357 | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 5 | |
| LACTOSE MONOHYDRATE | INACTIVE INGREDIENT | EWQ57Q8I5X | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 5 | |
| MAGNESIUM STEARATE | INACTIVE INGREDIENT | 70097M6I30 | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 5 | |
| POLYETHYLENE GLYCOLS | INACTIVE INGREDIENT | 3WJQ0SDW1A | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 5 | |
| POLYVINYL ALCOHOL | INACTIVE INGREDIENT | 532B59J990 | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 5 | |
| SODIUM STARCH GLYCOLATE TYPE A POTATO | INACTIVE INGREDIENT | 5856J3G2A2 | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 5 | |
| TALC | INACTIVE INGREDIENT | 7SEV7J4R1U | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 5 | |
| TITANIUM DIOXIDE | INACTIVE INGREDIENT | 15FIX9V2JP | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 5 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68084-602 | PERPHENAZINE TABLET, FILM COATED [AMERICAN HEALTH PACKAGING] | 13 | Current NDC, Legacy NDC, 2 package rows | 20241122_a17c90f9-3d5d-4503-ba2c-754b45decbf8.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68084-602-01 | 68084060201 | 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-602-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-602-11) | 100 blister pack | 2012-08-14 | 0000-00-00 | No | No | Current |
| 68084-602-11 | 68084060211 | 1 in 1 BLISTER PACK | | | | | | Historical |