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NDC 00781-2672-02 Calcium Acetate 667 mg/1 Details

Calcium Acetate 667 mg/1

Calcium Acetate is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sandoz Inc. The primary component is CALCIUM ACETATE.

MedlinePlus Drug Summary

Calcium acetate is used to control high blood levels of phosphorus in people with kidney disease who are on dialysis (medical treatment to clean the blood when the kidneys are not working properly). Calcium acetate is in a class of medications called phosphate binders. It binds phosphorus that you get from foods in your diet and prevents it from being absorbed into your blood stream.

Related Packages: 00781-2672-02
Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Calcium Acetate

Product Information

NDC	00781-2672
Product ID	0781-2672_07ffc7b1-97bd-09ba-e063-6294a90a521c
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	Calcium Acetate
Proprietary Name Suffix	n/a
Non-Proprietary Name	Calcium Acetate
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	CAPSULE
Route	ORAL
Active Ingredient Strength	667
Active Ingredient Units	mg/1
Substance Name	CALCIUM ACETATE
Labeler Name	Sandoz Inc
Pharmaceutical Class	Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA]
DEA Schedule	n/a
Marketing Category	NDA AUTHORIZED GENERIC
Application Number	NDA021160
Listing Certified Through	n/a

Package

NDC 00781-2672-02 (00781267202)

Pricing Information	N/A
NDC Package Code	0781-2672-02
Billing NDC	00781267202
Package	200 CAPSULE in 1 BOTTLE (0781-2672-02)
Marketing Start Date	2012-03-14
NDC Exclude Flag	N