Trifluoperazine Hydrochloride
- Product NDC
- 0781-8036
- 11-digit product format
- 007818036
- Labeler code
- 0781
- Product ID
- 0781-8036_79bbd43c-c3f3-4fa5-a2a4-88868251febb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trifluoperazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Sandoz Inc.
- Application
- ANDA085788
- Marketing category
- ANDA
- Marketing start
- 1981-11-20
- Substance
- TRIFLUOPERAZINE HYDROCHLORIDE
- Active strength
- 10 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
- Trifluoperazine Hydrochloride
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRIFLUOPERAZINE HYDROCHLORIDE | 10 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6P1Y2SNF5V |
| Rxcui | 198322, 198323, 198324, 198325 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0781-8036-01 | Trifluoperazine Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0781-8036 | TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED [SANDOZ INC.] | 7 | Current NDC, Legacy NDC, 1 package rows | 20250214_ae43c10e-cfa9-4298-8af5-7a3e6524bbda.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 |
|---|
| 0781-8036-01 | 00781803601 | 100 TABLET, FILM COATED in 1 BOTTLE (0781-8036-01) | 2019-01-14 | 0000-00-00 | No | No | Current |