Mirtazapine
- Product NDC
- 71335-0951
- 11-digit product format
- 713350951
- Labeler code
- 71335
- Product ID
- 71335-0951_92ebaf99-2450-431e-bfd8-ffd09d151fec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076307
- Marketing category
- ANDA
- Marketing start
- 2016-11-01
- Marketing end
- 0000-00-00
- Substance
- MIRTAZAPINE
- Active strength
- 30 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 |
|---|
| 71335-0951-1 | 71335095101 | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-0951-1) | 2018-09-21 | 0000-00-00 | No | No | Current |