Mirtazapine
- Product NDC
- 70518-1293
- 11-digit product format
- 705181293
- Labeler code
- 70518
- Product ID
- 70518-1293_eaeca762-db84-32ed-e053-2995a90a55a3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076921
- Marketing category
- ANDA
- Marketing start
- 2018-07-11
- Marketing end
- 0000-00-00
- Substance
- MIRTAZAPINE
- Active strength
- 45 mg/1
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-1293-0 | 70518129300 | 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1293-0) | 2018-07-11 | 0000-00-00 | No | No | Current |