Mirtazapine
- Product NDC
- 71335-1534
- 11-digit product format
- 713351534
- Labeler code
- 71335
- Product ID
- 71335-1534_535c1a04-956f-442b-a137-c7946bc448d0
- 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
- 2006-02-28
- Marketing end
- 0000-00-00
- Substance
- MIRTAZAPINE
- Active strength
- 45 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| A051Q2099Q | MIRTAZAPINE | 85650-52-8 | MIRTAZAPINE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 71335-1534-1 | 71335153401 | 30 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (71335-1534-1) | 2020-03-11 | 0000-00-00 | No | No | Current |