NDC 23155-531 – Calcium acetate

Calcium Acetate 667 mg/1 · Capsule · Oral

Human Prescription Drug 1 recall

Product NDC23155-531

Product details

Brand name
Calcium acetate
Generic name
Calcium acetate
Labeler
Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
Dosage form
Capsule
Route
Oral
Marketing category
ANDA · ANDA202315
Marketed since
July 7, 2015
Listing expires
December 31, 2026
Pharmacologic class
Blood Coagulation Factor; Phosphate Binder

Active ingredients

Uses, dosage, side effects and warnings for Calcium Acetate →

Package NDC codes (3)

Package NDCDescriptionSince
23155-531-02200 CAPSULE in 1 BOTTLE (23155-531-02)Jul 7, 2015
23155-531-101000 CAPSULE in 1 BOTTLE (23155-531-10)Jul 7, 2015
23155-531-1813600 CAPSULE in 1 CONTAINER (23155-531-18)Jul 7, 2015

Recalls mentioning this NDC

Other Calcium Acetate products