NDC 65862-006 – Citalopram
Citalopram Hydrobromide 20 mg/1 · Tablet, Film Coated · Oral
Product NDC65862-006
Product details
- Brand name
- Citalopram
- Generic name
- Citalopram Hydrobromide
- Labeler
- Aurobindo Pharma Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077031
- Marketed since
- October 28, 2004
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Citalopram Hydrobromide 20 mg/1
Package NDC codes (7)
| Package NDC | Description | Since |
|---|---|---|
| 65862-006-01 | 100 TABLET, FILM COATED in 1 BOTTLE (65862-006-01) | Oct 28, 2004 |
| 65862-006-05 | 500 TABLET, FILM COATED in 1 BOTTLE (65862-006-05) | Oct 28, 2004 |
| 65862-006-10 | 10 BLISTER PACK in 1 CARTON (65862-006-10) / 10 TABLET, FILM COATED in 1 BLISTER PACK | Oct 28, 2004 |
| 65862-006-30 | 30 TABLET, FILM COATED in 1 BOTTLE (65862-006-30) | Oct 28, 2004 |
| 65862-006-32 | 30 TABLET, FILM COATED in 1 BLISTER PACK (65862-006-32) | Oct 28, 2004 |
| 65862-006-60 | 60 TABLET, FILM COATED in 1 BOTTLE (65862-006-60) | Oct 28, 2004 |
| 65862-006-90 | 90 TABLET, FILM COATED in 1 BOTTLE (65862-006-90) | Oct 28, 2004 |
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