NDC 0378-6232 – Citalopram
Citalopram Hydrobromide 20 mg/1 · Tablet, Film Coated · Oral
Product NDC0378-6232
Product details
- Brand name
- Citalopram
- Generic name
- Citalopram
- Labeler
- Mylan Pharmaceuticals Inc.
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA077042
- Marketed since
- July 28, 2008
- Listing expires
- December 31, 2026
- Pharmacologic class
- Serotonin Reuptake Inhibitor
Active ingredients
- Citalopram Hydrobromide 20 mg/1
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 0378-6232-01 | 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6232-01) | Jul 28, 2008 |
| 0378-6232-05 | 500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-6232-05) | Jul 28, 2008 |
Recalls mentioning this NDC
- D-0173-2024 Jan 3, 2024 · Class II
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
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