Bupropion hydrochloride, Sr 200 mg / 1 Tablet 3600 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

bupropion hydrochloride, Sr NDC Family 71610-0582 bupropion hydrochloride, Sr 200 mg / 1

NDC 11	71610-0582-83
Product NDC	71610-0582
Generic Drug Name	bupropion hydrochloride, Sr
Brand Name	Bupropion Hydrochloride, Sr
Manufacturer	Aphena Pharma Solutions - Tennessee, LLC
Strength	200 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	3600 Tablet, Film Coated, Extended Release
Package Description	3600 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (71610-582-83)
Active Ingredients	Bupropion Hydrochloride
Marketing Category	ANDA

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NDC snapshot

bupropion hydrochloride, Sr 200 mg / 1 Tablet is tracked under NDC 71610-0582-83 and rolls up into product family 71610-0582. Use this page to confirm the exact presentation before comparing related family pages or starting a quote review.

Package configuration: 3600 Tablet, Film Coated, Extended Release.
Manufacturer: Aphena Pharma Solutions - Tennessee, LLC.
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familybupropion hydrochloride, Sr

Official references

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Bupropion hydrochloride, Sr 200 mg / 1 Tablet 3600 Tablet, Film Coated, Extended Release, NDC 71610-0582-83, is a Aphena Pharma Solutions - Tennessee, LLC 200 mg / 1 tablet presentation packaged as 3600 Tablet, Film Coated, Extended Release.

NDC search formats

Canonical NDC 11: 71610-0582-83
Digits-only NDC 11: 71610058283
Possible 10-digit display format: 71610-582-83 (7161058283)

Helpful product links

Search by brand name: Bupropion Hydrochloride, Sr
Exact NDC 11: 71610-0582-83
Product family NDC: 71610-0582
VA classification code: CN609
VA classification code description: ANTIDEPRESSANTS,OTHER
CMOP ID: B0538
VUID: 4024749