NDC 65862-079 – Terbinafine

Terbinafine Hydrochloride 250 mg/1 · Tablet · Oral

Human Prescription Drug

Product NDC65862-079

Product details

Brand name
Terbinafine
Generic name
Terbinafine Hydrochloride
Labeler
Aurobindo Pharma Limited
Dosage form
Tablet
Route
Oral
Marketing category
ANDA · ANDA078297
Marketed since
July 2, 2007
Listing expires
December 31, 2026
Pharmacologic class
Allylamine Antifungal

Active ingredients

Uses, dosage, side effects and warnings for Terbinafine →

Package NDC codes (3)

Package NDCDescriptionSince
65862-079-01100 TABLET in 1 BOTTLE (65862-079-01)Jul 2, 2007
65862-079-3030 TABLET in 1 BOTTLE (65862-079-30)Jul 2, 2007
65862-079-991000 TABLET in 1 BOTTLE (65862-079-99)Jul 2, 2007

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