Bupropion Hydrochloride 300 mg / 1 Tablet 500 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

Bupropion Hydrochloride NDC Family 63629-2138 Bupropion Hydrochloride 300 mg / 1

NDC 11	63629-2138-01
Product NDC	63629-2138
Generic Drug Name	Bupropion Hydrochloride
Brand Name	Bupropion Hydrochloride
Manufacturer	Bryant Ranch Prepack
Strength	300 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	500 Tablet, Film Coated, Extended Release
Package Description	500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-2138-1)
Active Ingredients	Bupropion Hydrochloride
Marketing Category	ANDA

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NDC snapshot

Bupropion Hydrochloride 300 mg / 1 Tablet is tracked under NDC 63629-2138-01 and rolls up into product family 63629-2138. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 500 Tablet, Film Coated, Extended Release.
Manufacturer: Bryant Ranch Prepack.
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familyBupropion Hydrochloride

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Bupropion Hydrochloride 300 mg / 1 Tablet 500 Tablet, Film Coated, Extended Release, NDC 63629-2138-01, is a Bryant Ranch Prepack 300 mg / 1 tablet presentation packaged as 500 Tablet, Film Coated, Extended Release.

NDC search formats

Canonical NDC 11: 63629-2138-01
Digits-only NDC 11: 63629213801
Possible 10-digit display format: 63629-2138-1 (6362921381)

Helpful product links

Search by brand name: Bupropion Hydrochloride
Exact NDC 11: 63629-2138-01
Product family NDC: 63629-2138
VA classification code: CN609
VA classification code description: ANTIDEPRESSANTS,OTHER
CMOP ID: B0586
VUID: 4026568