Mirtazapine
- Product NDC
- 68071-4045
- 11-digit product format
- 680714045
- Labeler code
- 68071
- Product ID
- 68071-4045_566a65be-4cf5-12fb-e054-00144ff88e88
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#