NDC 68788-0802 – Citalopram Hydrobromide
Citalopram Hydrobromide 20 mg/1 · Tablet, Film Coated · Oral
Product NDC68788-0802
Product details
- Brand name
- Citalopram Hydrobromide
- Generic name
- Citalopram Hydrobromide
- Labeler
- Preferred Pharmaceuticals, Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA078216
- Marketed since
- March 26, 2013
- Listing expires
- December 31, 2027
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Citalopram Hydrobromide 20 mg/1
Uses, dosage, side effects and warnings for Citalopram Hydrobromide →
Package NDC codes (5)
| Package NDC | Description | Since |
|---|---|---|
| 68788-0802-1 | 100 TABLET, FILM COATED in 1 BOTTLE (68788-0802-1) | Mar 26, 2013 |
| 68788-0802-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68788-0802-3) | Mar 26, 2013 |
| 68788-0802-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68788-0802-6) | Mar 26, 2013 |
| 68788-0802-8 | 120 TABLET, FILM COATED in 1 BOTTLE (68788-0802-8) | Mar 26, 2013 |
| 68788-0802-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68788-0802-9) | Mar 26, 2013 |
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