Pazopanib - Hydrochloride 200 mg / 1 Tablet 120 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

pazopanib hydrochloride NDC Family 82293-0022 pazopanib hydrochloride 200 mg / 1

NDC 11	82293-0022-10
Product NDC	82293-0022
Generic Drug Name	pazopanib hydrochloride
Brand Name	pazopanib
Manufacturer	Novugen Pharma (USA) LLC.
Strength	200 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	120 Tablet, Film Coated
Package Description	120 TABLET, FILM COATED in 1 BOTTLE (82293-022-10)
Active Ingredients	Pazopanib Hydrochloride
Marketing Category	ANDA

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NDC snapshot

pazopanib hydrochloride 200 mg / 1 Tablet is tracked under NDC 82293-0022-10 and rolls up into product family 82293-0022. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

Package configuration: 120 Tablet, Film Coated.
Manufacturer: Novugen Pharma (USA) LLC..
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Official references

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Potential alternatives with matching presentation

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View Potential Alternative Hubpazopanib hydrochloride 200 mg / 1 Tablet 120 Tablet, Film Coated Bottle2 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Votrient - Pazopanib hydrochloride 200 mg / 1 Tablet 120 Tablet, Film CoatedNDC 00078-1077-66 | 120 Tablet, Film Coated | Novartis Pharmaceuticals Corporation

Pazopanib - Hydrochloride 200 mg / 1 Tablet 120 Tablet, Film Coated, NDC 82293-0022-10, is a Novugen Pharma (USA) LLC. 200 mg / 1 tablet presentation packaged as 120 Tablet, Film Coated.

NDC search formats

Canonical NDC 11: 82293-0022-10
Digits-only NDC 11: 82293002210
Possible 10-digit display format: 82293-022-10 (8229302210)

Helpful product links

Search by brand name: pazopanib
NDC 11: 82293-0022-10
Product family NDC: 82293-0022
VA classification code: AN900
VA classification code description: ANTINEOPLASTIC,OTHER
CMOP ID: P0934
VUID: 4029446