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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 6P1Y2SNF5V | TRIFLUOPERAZINE HYDROCHLORIDE | 440-17-5 | TRIFLUOPERAZINE HYDROCHLORIDE |
Packages
| 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 |