Perphenazine
- Product NDC
- 70518-0731
- 11-digit product format
- 705180731
- Labeler code
- 70518
- Product ID
- 70518-0731_e21f8f80-a8b3-0927-e053-2995a90acaf8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Perphenazine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207582
- Marketing category
- ANDA
- Marketing start
- 2017-09-12
- Marketing end
- 0000-00-00
- Substance
- PERPHENAZINE
- Active strength
- 16 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 |
|---|
| 70518-0731-0 | 70518073100 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0731-0) | | 2017-09-12 | 0000-00-00 | No | No | Current |
| 70518-0731-1 | 70518073101 | 100 POUCH in 1 BOX, UNIT-DOSE (70518-0731-1) > 1 TABLET, FILM COATED in 1 POUCH (70518-0731-2) | 100 pouch | 2019-03-06 | 0000-00-00 | No | No | Current |