Mirtazapine
- Product NDC
- 43063-674
- 11-digit product format
- 430630674
- Labeler code
- 43063
- Product ID
- 43063-674_82e5d187-09b5-28e3-e053-2991aa0a105a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA076119
- Marketing category
- ANDA
- Marketing start
- 2003-01-29
- 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