NDC 65862-001 – Mirtazapine
Mirtazapine 7.5 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-001
Product details
- Brand name
- Mirtazapine
- Generic name
- Mirtazapine
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA076921
- Marketed since
- October 22, 2004
- Listing expires
- December 31, 2026
Active ingredients
- Mirtazapine 7.5 mg/1
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 65862-001-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-001-01) | Oct 22, 2004 |
| 65862-001-05 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-001-05) | Oct 22, 2004 |
| 65862-001-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-001-30) | Oct 22, 2004 |
| 65862-001-60 | 60 TABLET, FILM COATED in 1 BOTTLE (65862-001-60) | Oct 22, 2004 |
| 65862-001-90 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-001-90) | Oct 22, 2004 |
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