NDC 55111-782 – Fexofenadine hydrochloride
Fexofenadine Hydrochloride 30 mg/1 · Tablet · Oral
Product NDC55111-782
Product details
- Brand name
- Fexofenadine hydrochloride
- Generic name
- Fexofenadine hydrochloride
- Labeler
- Dr. Reddy's Laboratories Limited
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076502
- Marketed since
- January 3, 2011
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Fexofenadine Hydrochloride 30 mg/1
Uses, dosage, side effects and warnings for Fexofenadine Hydrochloride →
Package NDC codes (4)
| Package NDC | Description | Since |
|---|---|---|
| 55111-782-01 | 100 TABLET in 1 BOTTLE (55111-782-01) | Jan 3, 2011 |
| 55111-782-30 | 30 TABLET in 1 BOTTLE (55111-782-30) | Jan 3, 2011 |
| 55111-782-78 | 10 BLISTER PACK in 1 CARTON (55111-782-78) / 10 TABLET in 1 BLISTER PACK (55111-782-79) | Jan 3, 2011 |
| 55111-782-90 | 90 TABLET in 1 BOTTLE (55111-782-90) | Jan 3, 2011 |
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