NDC codes

FDA NDC Directory
Product NDC (as listed)60687-589Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60687-0589Add 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
60687-589-65606870589656068705896550 BLISTER PACK in 1 CARTON (60687-589-65) / 1 CAPSULE in 1 BLISTER PACK (60687-589-11)Marketed from Jul 5, 2026

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
American Health PackagingNDC labeler code 60687
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203135
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 60687-589_5aaba361-3fc5-712f-e063-6294a90a39f0SPL ID 5aaba361-3fc5-712f-e063-6294a90a39f0SPL set ID 2072d9f4-abb1-4699-bde5-6041dd79cad5RxCUI 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

N460687058965 followed by a unit qualifier and the quantity

Package 60687-0589-65. 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 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)

About NDC 60687-589

What is NDC 60687-589?
60687-589 is the product NDC for Calcium Acetate, Calcium acetate 667 mg/1 capsule, listed with the FDA by American Health Packaging. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Calcium Acetate.
What is the active ingredient?
Calcium acetate.
Who is the labeler?
American Health Packaging, NDC labeler code 60687. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Calcium Acetate?
21 other product NDCs are listed under this name. See all Calcium Acetate NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Calcium Acetate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Calcium AcetateCalcium acetate 667 mg/1CapsuleOralAvPAK50268-20350268-0203-15
Calcium AcetateCalcium acetate 667 mg/1CapsuleOralWestminster Pharmaceuticals, LLC69367-41169367-0411-02
Calcium AcetateCalcium acetate 667 mg/1CapsuleOralProficient Rx LP82804-96882804-0968-0082804-0968-2082804-0968-30+6 more
calcium acetateCalcium acetate 667 mg/1CapsuleOralAvKARE73190-03173190-0031-20
calcium acetateCalcium acetate 667 mg/1CapsuleOralREMEDYREPACK INC.70518-429970518-4299-00
Calcium AcetateCalcium acetate 667 mg/1CapsuleOralNCS HealthCare of KY, LLC dba Vangard Labs0615-863200615-8632-39
Calcium AcetateCalcium acetate 667 mg/1CapsuleOralPD-Rx Pharmaceuticals, Inc.72789-42272789-0422-97
Calcium AcetateCalcium acetate 667 mg/1CapsuleOralNivagen Pharmaceuticals, Inc.75834-32375834-0323-02
Calcium AcetateCalcium acetate 667 mg/1CapsuleOralSQUARE PHARMACEUTICALS LIMITED76483-08676483-0086-00
Calcium AcetateCalcium acetate 667 mg/1CapsuleOralRising Pharma Holdings, Inc.16571-81316571-0813-20

All 22 Calcium Acetate NDCs

Other NDCs under ANDA 203135

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

FDA NDC Directory listings under ANDA 203135
ProductStrengthForm · routeLabelerProduct NDC
Calcium AcetateCalcium acetate 667 mg/1CapsuleOralCipla USA Inc.,69097-862
Calcium AcetateCalcium acetate 667 mg/1CapsuleOralEXELAN PHARMACEUTICALS, INC.76282-377

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