Mirtazapine
- Product NDC
- 71335-2963
- 11-digit product format
- 713352963
- Labeler code
- 71335
- Product ID
- 71335-2963_4252f585-b169-a518-e063-6394a90a04b6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mirtazapine
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076541
- Marketing category
- ANDA
- Marketing start
- 2004-04-22
- Substance
- MIRTAZAPINE
- Active strength
- 30 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| A051Q2099Q | MIRTAZAPINE | 85650-52-8 | MIRTAZAPINE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2963-1 | 71335296301 | 500 TABLET in 1 BOTTLE (71335-2963-1) | 500 tablet | 2025-10-29 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Mirtazapine | Bryant Ranch Prepack | 2025-10-29 | HUMAN PRESCRIPTION DRUG LABEL | 100 |