Perphenazine
- Product NDC
- 70518-0458
- 11-digit product format
- 705180458
- Labeler code
- 70518
- Product ID
- 70518-0458_e1a4eef7-9a3a-0f7d-e053-2a95a90ac9d8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040226
- Marketing category
- ANDA
- Marketing start
- 2017-04-24
- Marketing end
- 0000-00-00
- Substance
- PERPHENAZINE
- Active strength
- 8 mg/1
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0458-0 | 70518045800 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0458-0) | | 2017-04-24 | 0000-00-00 | No | No | Current |
| 70518-0458-1 | 70518045801 | 100 POUCH in 1 BOX (70518-0458-1) > 1 TABLET, FILM COATED in 1 POUCH (70518-0458-2) | 100 pouch | 2022-02-23 | 0000-00-00 | No | No | Current |