Bupropion Hydrochloride 75 mg / 1 Tablet 30 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

Bupropion Hydrochloride NDC Family 70518-1566 Bupropion Hydrochloride 75 mg / 1

NDC 11	70518-1566-00
Product NDC	70518-1566
Generic Drug Name	Bupropion Hydrochloride
Brand Name	Bupropion Hydrochloride
Manufacturer	Remedyrepack Inc.
Strength	75 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	30 Tablet, Film Coated
Package Description	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1566-0)
Active Ingredients	Bupropion Hydrochloride
Marketing Category	ANDA

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NDC snapshot

Bupropion Hydrochloride 75 mg / 1 Tablet is tracked under NDC 70518-1566-00 and rolls up into product family 70518-1566. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 30 Tablet, Film Coated.
Manufacturer: Remedyrepack Inc..
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familyBupropion Hydrochloride

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Bupropion Hydrochloride 75 mg / 1 Tablet 30 Tablet, Film Coated, NDC 70518-1566-00, is a Remedyrepack Inc. 75 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated.

NDC search formats

Canonical NDC 11: 70518-1566-00
Digits-only NDC 11: 70518156600
Possible 10-digit display format: 70518-1566-0 (7051815660)

Helpful product links

Search by brand name: Bupropion Hydrochloride
Exact NDC 11: 70518-1566-00
Product family NDC: 70518-1566
VA classification code: CN609
VA classification code description: ANTIDEPRESSANTS,OTHER
CMOP ID: B0194
VUID: 4008986