Terbinafine hydrochloride 250 mg / 1 Tablet 45 Tablet

Reference details for licensed healthcare facility review and verification.

terbinafine hydrochloride NDC Family 70518-3907 terbinafine hydrochloride 250 mg / 1

NDC 11	70518-3907-02
Product NDC	70518-3907
Generic Drug Name	terbinafine hydrochloride
Brand Name	terbinafine hydrochloride
Manufacturer	Remedyrepack Inc.
Strength	250 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	45 Tablet
Package Description	45 TABLET in 1 BOTTLE, PLASTIC (70518-3907-2)
Active Ingredients	Terbinafine Hydrochloride
Marketing Category	ANDA

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NDC snapshot

terbinafine hydrochloride 250 mg / 1 Tablet is tracked under NDC 70518-3907-02 and rolls up into product family 70518-3907. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 45 Tablet.
Manufacturer: Remedyrepack Inc..
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familyterbinafine hydrochloride

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Terbinafine hydrochloride 250 mg / 1 Tablet 45 Tablet, NDC 70518-3907-02, is a Remedyrepack Inc. 250 mg / 1 tablet presentation packaged as 45 Tablet.

NDC search formats

Canonical NDC 11: 70518-3907-02
Digits-only NDC 11: 70518390702
Possible 10-digit display format: 70518-3907-2 (7051839072)

Helpful product links

Search by brand name: terbinafine hydrochloride
Exact NDC 11: 70518-3907-02
Product family NDC: 70518-3907
VA classification code: AM700
VA classification code description: ANTIFUNGALS
CMOP ID: T0356
VUID: 4010294