Mirtazapine
- Product NDC
- 58118-0052
- 11-digit product format
- 581180052
- Labeler code
- 58118
- Product ID
- 58118-0052_b026108d-acc9-4ebe-e053-2a95a90af27c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Clinical Solutions Wholesale, 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
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 58118-0052-8 | 58118005208 | 30 TABLET, FILM COATED in 1 BLISTER PACK (58118-0052-8) | 2015-09-24 | 0000-00-00 | No | No | Current |