Mirtazapine
- Product NDC
- 0591-2470
- 11-digit product format
- 005912470
- Labeler code
- 0591
- Product ID
- 0591-2470_28133a24-c62b-4e1d-9246-d825c2c93585
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Actavis Pharma, Inc.
- Application
- ANDA076307
- Marketing category
- ANDA
- Marketing start
- 2014-02-11
- Marketing end
- 2019-08-31
- Substance
- MIRTAZAPINE
- Active strength
- 30 mg/1
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record