Mirtazapine
- Product NDC
- 72162-1639
- 11-digit product format
- 721621639
- Labeler code
- 72162
- Product ID
- 72162-1639_53386747-10e4-48e2-9ab0-e4bfe4eddfa5
- 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
- 15 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 |
|---|
| 72162-1639-0 | 72162163900 | 1000 TABLET in 1 BOTTLE (72162-1639-0) | 1000 tablet | 2023-08-28 | No | No | Historical |
| 72162-1639-3 | 72162163903 | 30 TABLET in 1 BOTTLE (72162-1639-3) | 30 tablet | 2023-08-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Mirtazapine | Bryant Ranch Prepack | 2023-08-28 | HUMAN PRESCRIPTION DRUG LABEL | 100 |