fluvoxamine maleate
- Product NDC
- 70518-1789
- 11-digit product format
- 705181789
- Labeler code
- 70518
- Product ID
- 70518-1789_d9f741c3-4351-1351-e053-2a95a90a9a8f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluvoxamine maleate
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- NDA021519
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2019-01-11
- Marketing end
- 0000-00-00
- Substance
- FLUVOXAMINE MALEATE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 70518-1789 | FLUVOXAMINE MALEATE TABLET, COATED [REMEDYREPACK INC.] | 9 | Legacy NDC | 20240224_87f87cac-5369-45e4-8d66-c6dedcb51f3e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1789-1 | 70518178901 | 100 POUCH in 1 BOX (70518-1789-1) > 1 TABLET, COATED in 1 POUCH (70518-1789-0) | 100 pouch | 2019-01-11 | 0000-00-00 | No | No | Current |