NDC 87063-220 – Citalopram
Citalopram Hydrobromide 20 mg/1 · Tablet, Film Coated · Oral
Product NDC87063-220
Product details
- Brand name
- Citalopram
- Generic name
- Citalopram
- Labeler
- ASCLEMED USA INC.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078216
- Marketed since
- October 18, 2007
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Citalopram Hydrobromide 20 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 87063-220-01 | 100 TABLET, FILM COATED in 1 BOTTLE (87063-220-01) | May 29, 2026 |
| 87063-220-10 | 10 TABLET, FILM COATED in 1 BOTTLE (87063-220-10) | May 29, 2026 |
| 87063-220-20 | 20 TABLET, FILM COATED in 1 BOTTLE (87063-220-20) | May 29, 2026 |
| 87063-220-30 | 30 TABLET, FILM COATED in 1 BOTTLE (87063-220-30) | May 29, 2026 |
| 87063-220-60 | 60 TABLET, FILM COATED in 1 BOTTLE (87063-220-60) | May 29, 2026 |
| 87063-220-90 | 90 TABLET, FILM COATED in 1 BOTTLE (87063-220-90) | May 29, 2026 |
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