NDC 55111-782 – Fexofenadine hydrochloride

Fexofenadine Hydrochloride 30 mg/1 · Tablet · Oral

Human Otc Drug

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

Uses, dosage, side effects and warnings for Fexofenadine Hydrochloride →

Package NDC codes (4)

Package NDCDescriptionSince
55111-782-01100 TABLET in 1 BOTTLE (55111-782-01)Jan 3, 2011
55111-782-3030 TABLET in 1 BOTTLE (55111-782-30)Jan 3, 2011
55111-782-7810 BLISTER PACK in 1 CARTON (55111-782-78) / 10 TABLET in 1 BLISTER PACK (55111-782-79)Jan 3, 2011
55111-782-9090 TABLET in 1 BOTTLE (55111-782-90)Jan 3, 2011

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