Fluphenazine Hydrochloride
- Product NDC
- 70518-3553
- 11-digit product format
- 705183553
- Labeler code
- 70518
- Product ID
- 70518-3553_f0d4654d-fd55-3bf3-e053-2a95a90acd4a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluphenazine Hydrochloride
- Dosage form
- SOLUTION, CONCENTRATE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA074725
- Marketing category
- ANDA
- Marketing start
- 2022-10-11
- Marketing end
- 0000-00-00
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 5 mg/mL
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3553-0 | 70518355300 | 10 CUP, UNIT-DOSE in 1 BOX (70518-3553-0) > 1 mL in 1 CUP, UNIT-DOSE (70518-3553-1) | 2022-10-11 | 0000-00-00 | No | No | Current |