NDC 68016-995 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 180 mg/1 · Tablet · Oral
Product NDC68016-995
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine hydrochloride
- Labeler
- Chain Drug Consortium, LLC
- Dosage form
- Tablet
- Route
- Oral
- Marketing category
- ANDA · ANDA076502
- Marketed since
- April 1, 2014
- Listing expires
- December 31, 2026
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Fexofenadine Hydrochloride 180 mg/1
Uses, dosage, side effects and warnings for Fexofenadine Hydrochloride →
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 68016-995-03 | 1 BOTTLE in 1 CARTON (68016-995-03) / 30 TABLET in 1 BOTTLE | Apr 1, 2014 |
| 68016-995-45 | 1 BOTTLE in 1 CARTON (68016-995-45) / 45 TABLET in 1 BOTTLE | Apr 1, 2014 |
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