NDC 55111-250 – Terbinafine Hydrochloride

Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC55111-250

Product details

Brand name
Terbinafine Hydrochloride
Generic name
Terbinafine Hydrochloride
Labeler
Dr.Reddys Laboratories Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA076390
Marketed since
July 2, 2007
Listing expires
December 31, 2026
Pharmacologic class
Allylamine Antifungal

Active ingredients

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

Package NDC codes (5)

Package NDCDescriptionSince
55111-250-01100 TABLET in 1 BOTTLE (55111-250-01)Jul 2, 2007
55111-250-05500 TABLET in 1 BOTTLE (55111-250-05)Jul 2, 2007
55111-250-3030 TABLET in 1 BOTTLE (55111-250-30)Jul 2, 2007
55111-250-7910 BLISTER PACK in 1 CARTON (55111-250-79) / 10 TABLET in 1 BLISTER PACK (55111-250-78)Jul 2, 2007
55111-250-9090 TABLET in 1 BOTTLE (55111-250-90)Jul 2, 2007

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