Deferiprone 500 mg / 1 Tablet 100 Tablet

Reference details for licensed healthcare facility review and verification.

Deferiprone NDC Family 51672-4196 Deferiprone 500 mg / 1

NDC 11	51672-4196-01
Product NDC	51672-4196
Generic Drug Name	Deferiprone
Brand Name	Deferiprone
Manufacturer	Sun Pharmaceutical Industries, Inc.
Strength	500 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	100 Tablet
Package Description	100 TABLET in 1 BOTTLE (51672-4196-1)
Active Ingredients	Deferiprone
Marketing Category	ANDA

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NDC snapshot

Deferiprone 500 mg / 1 Tablet is tracked under NDC 51672-4196-01 and rolls up into product family 51672-4196. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

Package configuration: 100 Tablet.
Manufacturer: Sun Pharmaceutical Industries, Inc..
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Review the generic familyDeferiprone

Official references

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Deferiprone 500 mg / 1 Tablet 100 Tablet, NDC 51672-4196-01, is a Sun Pharmaceutical Industries, Inc. 500 mg / 1 tablet presentation packaged as 100 Tablet.

NDC search formats

Canonical NDC 11: 51672-4196-01
Digits-only NDC 11: 51672419601
Possible 10-digit display format: 51672-4196-1 (5167241961)

Helpful product links

Search by brand name: Deferiprone
NDC 11: 51672-4196-01
Product family NDC: 51672-4196
VA classification code: AD300
VA classification code description: HEAVY METAL ANTAGONISTS
CMOP ID: D0913
VUID: 4031144