Trifluoperazine Hydrochloride
- Product NDC
- 70518-2095
- 11-digit product format
- 705182095
- Labeler code
- 70518
- Product ID
- 70518-2095_499dd16d-513b-780e-e063-6294a90a0230
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- trifluoperazine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040209
- Marketing category
- ANDA
- Marketing start
- 2019-05-21
- Substance
- TRIFLUOPERAZINE HYDROCHLORIDE
- Active strength
- 2 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Trifluoperazine Hydrochloride
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRIFLUOPERAZINE HYDROCHLORIDE | 2 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6P1Y2SNF5V |
| Rxcui | 198324 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-2095-0 | Trifluoperazine Hydrochloride | 30 in 1 BLISTER PACK | TABLET, FILM COATED | 30 | | 12 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-2095 | TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED [REMEDYREPACK INC.] | 10 | Current NDC, Legacy NDC, 1 package rows | 20250306_339ceb53-3b1c-459f-84eb-77bd4315c998.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 |
|---|
| 70518-2095-0 | 70518209500 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2095-0) | 2019-05-21 | 0000-00-00 | No | No | Current |