Fluvoxamine maleate
- Product NDC
- 70518-3153
- 11-digit product format
- 705183153
- Labeler code
- 70518
- Product ID
- 70518-3153_e95983a1-b2af-dc53-e053-2a95a90afbc3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluvoxamine maleate
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA075888
- Marketing category
- ANDA
- Marketing start
- 2021-07-14
- Marketing end
- 0000-00-00
- Substance
- FLUVOXAMINE MALEATE
- Active strength
- 50 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-3153-0 | 70518315300 | 100 POUCH in 1 BOX (70518-3153-0) > 1 TABLET, FILM COATED in 1 POUCH (70518-3153-1) | 100 pouch | 2021-07-14 | 0000-00-00 | No | No | Current |