fluphenazine hydrochloride
- Product NDC
- 70518-3003
- 11-digit product format
- 705183003
- Labeler code
- 70518
- Product ID
- 70518-3003_d3d1d886-960b-13a2-e053-2a95a90a9010
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- fluphenazine hydrochloride
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA213647
- Marketing category
- ANDA
- Marketing start
- 2021-01-29
- Marketing end
- 0000-00-00
- Substance
- FLUPHENAZINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Phenothiazines [CS],Phenothiazine [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3003-0 | 70518300300 | 100 POUCH in 1 BOX (70518-3003-0) > 1 TABLET, FILM COATED in 1 POUCH (70518-3003-1) | 100 pouch | 2021-01-29 | 0000-00-00 | No | No | Current |