Mirtazapine
- Product NDC
- 55700-341
- 11-digit product format
- 557000341
- Labeler code
- 55700
- Product ID
- 55700-341_2926edcb-c68f-4f4d-a5a8-f15fb3b99c9f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical Medical DBA Quality Care Products LLC
- Application
- ANDA077666
- Marketing category
- ANDA
- Marketing start
- 2007-08-22
- 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