NDC codes

FDA NDC Directory
Product NDC (as listed)73190-031Labeler and product segments. Claims need a package NDC.
Product NDC at billing width73190-0031Add 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 NDC11-digit (billing)PackageCopy
73190-031-2073190003120200 CAPSULE in 1 BOTTLE (73190-031-20)Marketed from May 21, 2025

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 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
AvKARE
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202315
Marketing start
Listing expires
Other FDA classes
Calcium (Chemical structure)Divalent (Chemical structure)Increased Coagulation Factor Activity (Physiologic effect)Phosphate Chelating Activity (Mechanism)
Identifiers
Product ID 73190-031_35a6eb8e-624d-2222-e063-6394a90ab589SPL ID 35a6eb8e-624d-2222-e063-6394a90ab589SPL set ID 35a6f515-dfe7-031c-e063-6294a90a5e95RxCUI 359296UNII Y882YXF34XUPC 0373190031209
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

N473190003120 followed by a unit qualifier and the quantity

Package 73190-0031-20. 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 .

Indications (excerpt from the label)

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

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 202315

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

FDA NDC Directory listings under ANDA 202315
ProductStrengthForm · routeLabelerProduct NDC
calcium acetateCalcium acetate 667 mg/1CapsuleOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-531
calcium acetateCalcium acetate 667 mg/1CapsuleOralREMEDYREPACK INC.70518-4299

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