Ferric Citrate 210 mg / 1 Tablet 200 Tablet, Film Coated

Reference details for licensed healthcare facility review and verification.

Ferric Citrate NDC Family 00378-2895 Ferric Citrate 210 mg / 1

NDC 11	00378-2895-20
Product NDC	00378-2895
Generic Drug Name	Ferric Citrate
Brand Name	Ferric Citrate
Manufacturer	Mylan Pharmaceuticals Inc.
Strength	210 mg / 1
Dosage Form	Tablet
Drug Type	Oral
Package Quantity	200 Tablet, Film Coated
Package Description	200 TABLET, FILM COATED in 1 BOTTLE (0378-2895-20)
Active Ingredients	Tetraferric Tricitrate Decahydrate
Marketing Category	NDA AUTHORIZED GENERIC

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NDC snapshot

Ferric Citrate 210 mg / 1 Tablet is tracked under NDC 00378-2895-20 and rolls up into product family 00378-2895. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.

Package configuration: 200 Tablet, Film Coated.
Manufacturer: Mylan Pharmaceuticals Inc..
Dosage form: Tablet.
Family size: 1 indexed presentation.

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Potential alternatives with matching presentation

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View Potential Alternative Hubferric citrate 210 mg / 1 Tablet 200 Tablet, Film Coated Bottle2 package-level listings in the comparison hub.

Sample package-level pages in this comparison set

Auryxia - Ferric citrate 210 mg / 1 Tablet 200 Tablet, Film CoatedNDC 59922-0631-01 | 200 Tablet, Film Coated | Akebia Therapeutics, Inc.

Ferric Citrate 210 mg / 1 Tablet 200 Tablet, Film Coated, NDC 00378-2895-20, is a Mylan Pharmaceuticals Inc. 210 mg / 1 tablet presentation packaged as 200 Tablet, Film Coated.

NDC search formats

Canonical NDC 11: 00378-2895-20
Digits-only NDC 11: 00378289520
Possible 10-digit display format: 0378-2895-20 (0378289520)

Helpful product links

Search by brand name: Ferric Citrate
NDC 11: 00378-2895-20
Product family NDC: 00378-2895
VA classification code: TN410
VA classification code description: IRON
CMOP ID: F0543
VUID: 4033769