Mirtazapine
- Product NDC
- 70518-1583
- 11-digit product format
- 705181583
- Labeler code
- 70518
- Product ID
- 70518-1583_9484e4c0-df97-37a0-e053-2995a90a0ccd
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076541
- Marketing category
- ANDA
- Marketing start
- 2018-10-24
- Marketing end
- 0000-00-00
- Substance
- MIRTAZAPINE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record