NDC 62207-889 – Fexofenadine Hydrochloride
Fexofenadine Hydrochloride 60 mg/1 · Tablet, Film Coated · Oral
Product NDC62207-889
Product details
- Brand name
- Fexofenadine Hydrochloride
- Generic name
- Fexofenadine Hydrochloride
- Labeler
- Granules India Limited
- Dosage form
- Tablet, Film Coated
- Route
- Oral
- Marketing category
- ANDA · ANDA211075
- Marketed since
- November 7, 2023
- Listing expires
- December 31, 2027
- Pharmacologic class
- Histamine-1 Receptor Antagonist
Active ingredients
- Fexofenadine Hydrochloride 60 mg/1
Uses, dosage, side effects and warnings for Fexofenadine Hydrochloride →
Package NDC codes (3)
| Package NDC | Description | Since |
|---|---|---|
| 62207-889-49 | 1000 TABLET, FILM COATED in 1 BOTTLE (62207-889-49) | Nov 7, 2023 |
| 62207-889-51 | 1 BOTTLE in 1 CARTON (62207-889-51) / 10 TABLET, FILM COATED in 1 BOTTLE | Nov 7, 2023 |
| 62207-889-60 | 8 BLISTER PACK in 1 CARTON (62207-889-60) / 9 TABLET, FILM COATED in 1 BLISTER PACK | Nov 7, 2023 |
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