Mirtazapine
- Product NDC
- 70518-0901
- 11-digit product format
- 705180901
- Labeler code
- 70518
- Product ID
- 70518-0901_8f0876e4-ca7c-f0fc-e053-2a95a90a6408
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA076119
- Marketing category
- ANDA
- Marketing start
- 2017-12-12
- 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