Calcium Acetate NDC 0904-7119

NDC codes

FDA NDC Directory

Product NDC (as listed)0904-7119Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00904-7119Add the package segment from the table below.

Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC	11-digit (billing)	Package	Copy
0904-7119-06	00904711906	50 BLISTER PACK in 1 CARTON (0904-7119-06) / 1 CAPSULE in 1 BLISTER PACKMarketed from Feb 26, 2008
0904-7119-61	00904711961	100 BLISTER PACK in 1 CARTON (0904-7119-61) / 1 CAPSULE in 1 BLISTER PACKMarketed from Feb 26, 2008

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary): Calcium Acetate
Generic name (nonproprietary): calcium acetate
Active ingredients: Calcium acetate — 667 mg/1
Dosage form: Capsule
Route: Oral
Labeler: Major Pharmaceuticals
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 077728
Marketing start: Feb 26, 2008
Listing expires: Dec 31, 2027
Other FDA classes: Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers: Product ID 0904-7119_ff2e23f6-ba35-4bb1-80ef-feba4ae00bc2SPL ID ff2e23f6-ba35-4bb1-80ef-feba4ae00bc2SPL set ID 9a731cdf-6488-44ca-b97f-512a0e9deab1RxCUI 359296UNII Y882YXF34X
Pharmacologic class: Blood Coagulation Factor; Phosphate Binder

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N400904711906 followed by a unit qualifier and the quantity

Package 00904-7119-06. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective Mar 17, 2026.

Indications (excerpt from the label)

Calcium acetate is a phosphate binder indicated to reduce serum phosphorus in patients with end stage renal disease (ESRD). • Calcium acetate is a phosphate binder indicated for the reduction of serum phosphorus in patients with end stage renal disease. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 077728

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under ANDA 077728
Product	Strength	Form · route	Labeler	Product NDC
Calcium Acetate	Calcium acetate 667 mg/1	CapsuleOral	Cardinal Health 107, LLC	55154-4169
Calcium Acetate	Calcium acetate 667 mg/1	CapsuleOral	American Health Packaging	68084-479
Calcium Acetate	Calcium acetate 667 mg/1	CapsuleOral	Hikma Pharmaceuticals USA Inc.	0054-0088