Mirtazapine
- Product NDC
- 71335-0717
- 11-digit product format
- 713350717
- Labeler code
- 71335
- Product ID
- 71335-0717_bdad6478-a70e-4edb-8efb-33266071483f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA077376
- Marketing category
- ANDA
- Marketing start
- 2005-12-08
- Marketing end
- 0000-00-00
- Substance
- MIRTAZAPINE
- Active strength
- 15 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 71335-0717-1 | 71335071701 | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0717-1) | 2018-03-06 | 0000-00-00 | No | No | Current |
| 71335-0717-2 | 71335071702 | 1 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0717-2) | 2018-03-06 | 0000-00-00 | No | No | Current |
| 71335-0717-3 | 71335071703 | 29 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0717-3) | 2018-03-06 | 0000-00-00 | No | No | Current |