Ropinirole hydrochloride 12 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release

Reference details for licensed healthcare facility review and verification.

ropinirole hydrochloride NDC Family 42291-0717 ropinirole hydrochloride 12 mg / 1

NDC 11	42291-0717-30
Product NDC	42291-0717
Generic Drug Name	ropinirole hydrochloride
Brand Name	Ropinirole Hydrochloride
Manufacturer	AvKARE
Strength	12 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	30 Tablet, Film Coated, Extended Release
Package Description	30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-717-30)
Active Ingredients	Ropinirole Hydrochloride
Marketing Category	ANDA

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NDC snapshot

ropinirole hydrochloride 12 mg / 1 Tablet is tracked under NDC 42291-0717-30 and rolls up into product family 42291-0717. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

Package configuration: 30 Tablet, Film Coated, Extended Release.
Manufacturer: AvKARE.
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familyropinirole hydrochloride

Official references

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Ropinirole hydrochloride 12 mg / 1 Tablet 30 Tablet, Film Coated, Extended Release, NDC 42291-0717-30, is a AvKARE 12 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated, Extended Release.

NDC search formats

Canonical NDC 11: 42291-0717-30
Digits-only NDC 11: 42291071730
Possible 10-digit display format: 42291-717-30 (4229171730)

Helpful product links

Search by brand name: Ropinirole Hydrochloride
NDC 11: 42291-0717-30
Product family NDC: 42291-0717
VA classification code: CN500
VA classification code description: ANTIPARKINSON AGENTS
CMOP ID: R0257
VUID: 4028517