NDC 68071-3357 – Citalopram
Citalopram Hydrobromide 40 mg/1 · Tablet, Film Coated · Oral
Product NDC68071-3357
Product details
- Brand name
- Citalopram
- Generic name
- Citalopram Hydrobromide
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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 40 mg/1
Package NDC codes (6)
| Package NDC | Description | Since |
|---|---|---|
| 68071-3357-1 | 15 TABLET, FILM COATED in 1 BOTTLE (68071-3357-1) | Jul 14, 2017 |
| 68071-3357-3 | 30 TABLET, FILM COATED in 1 BOTTLE (68071-3357-3) | Jul 14, 2017 |
| 68071-3357-4 | 40 TABLET, FILM COATED in 1 BOTTLE (68071-3357-4) | Jul 14, 2017 |
| 68071-3357-5 | 45 TABLET, FILM COATED in 1 BOTTLE (68071-3357-5) | Jul 14, 2017 |
| 68071-3357-6 | 60 TABLET, FILM COATED in 1 BOTTLE (68071-3357-6) | Jul 14, 2017 |
| 68071-3357-9 | 90 TABLET, FILM COATED in 1 BOTTLE (68071-3357-9) | Jul 14, 2017 |
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