perphenazine
- Product NDC
- 70518-3121
- 11-digit product format
- 705183121
- Labeler code
- 70518
- Product ID
- 70518-3121_f15f6c59-d08c-2d63-e053-2a95a90abbaa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- perphenazine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA205232
- Marketing category
- ANDA
- Marketing start
- 2021-06-15
- Marketing end
- 0000-00-00
- Substance
- PERPHENAZINE
- Active strength
- 4 mg/1
- Pharmacologic classes
- Phenothiazine [EPC], Phenothiazines [CS]
- NDC exclude flag
- No
- Listing certified through
- 2024-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3121 | PERPHENAZINE TABLET [REMEDYREPACK INC.] | 3 | Legacy NDC | 20240314_5cf6073e-d6f9-41c1-a6c4-106acb20e50b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3121-0 | 70518312100 | 30 TABLET in 1 BLISTER PACK (70518-3121-0) | 30 tablet | 2021-06-15 | 0000-00-00 | No | No | Current |