NDC 71335-0664 – Mirtazapine
Mirtazapine 15 mg/1 · Tablet, Film Coated · Oral
Product NDC71335-0664
Product details
- Brand name
- Mirtazapine
- Generic name
- Mirtazapine
- Labeler
- Bryant Ranch Prepack
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076921
- Marketed since
- August 17, 2009
- Listing expires
- December 31, 2026
Active ingredients
- Mirtazapine 15 mg/1
Package NDC codes (8)
| Package NDC | Description | Since |
|---|---|---|
| 71335-0664-1 | 30 TABLET, FILM COATED in 1 BOTTLE (71335-0664-1) | May 31, 2019 |
| 71335-0664-2 | 60 TABLET, FILM COATED in 1 BOTTLE (71335-0664-2) | Sep 11, 2019 |
| 71335-0664-3 | 90 TABLET, FILM COATED in 1 BOTTLE (71335-0664-3) | Sep 13, 2019 |
| 71335-0664-4 | 120 TABLET, FILM COATED in 1 BOTTLE (71335-0664-4) | Apr 3, 2024 |
| 71335-0664-5 | 15 TABLET, FILM COATED in 1 BOTTLE (71335-0664-5) | Nov 18, 2021 |
| 71335-0664-6 | 180 TABLET, FILM COATED in 1 BOTTLE (71335-0664-6) | Apr 3, 2024 |
| 71335-0664-7 | 45 TABLET, FILM COATED in 1 BOTTLE (71335-0664-7) | Apr 3, 2024 |
| 71335-0664-8 | 21 TABLET, FILM COATED in 1 BOTTLE (71335-0664-8) | Apr 3, 2024 |
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