Trifluoperazine Hydrochloride
- Product NDC
- 72162-2207
- 11-digit product format
- 721622207
- Labeler code
- 72162
- Product ID
- 72162-2207_7be0a6fa-a2a0-4f9d-94ca-47ab51de9c1d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Trifluoperazine Hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA085789
- Marketing category
- ANDA
- Marketing start
- 1981-11-20
- Marketing end
- 2027-03-19
- Substance
- TRIFLUOPERAZINE HYDROCHLORIDE
- Active strength
- 5 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Trifluoperazine Hydrochloride
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| TRIFLUOPERAZINE HYDROCHLORIDE | 5 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6P1Y2SNF5V |
| Rxcui | 198325 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-2207-1 | Trifluoperazine Hydrochloride | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | | 101 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-2207 | TRIFLUOPERAZINE HYDROCHLORIDE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 101 | Current NDC, 1 package rows | 20240406_7be0a6fa-a2a0-4f9d-94ca-47ab51de9c1d.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 |
|---|
| 72162-2207-1 | 72162220701 | 100 TABLET, FILM COATED in 1 BOTTLE (72162-2207-1) | 2024-04-02 | 2027-03-19 | No | No | Historical |