NDC codes

FDA NDC Directory
Product NDC (as listed)67877-257Labeler and product segments. Claims need a package NDC.
Product NDC at billing width67877-0257Add 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
67877-257-90678770257906 BOTTLE in 1 CARTON (67877-257-90) / 15 TABLET, CHEWABLE in 1 BOTTLE (67877-257-15)Marketed from May 10, 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)
Lanthanum Carbonate
Generic name (nonproprietary)
lanthanum carbonate
Active ingredients
Lanthanum carbonate — 750 mg/1
Dosage form
Tablet, Chewable
Route
Oral
Labeler
Ascend Laboratories, LLCNDC labeler code 67877
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 202329
Marketing start
Listing expires
Other FDA classes
Phosphate Chelating Activity (Mechanism)
Identifiers
Product ID 67877-257_ba371296-8731-4ffa-ab36-aff022e48d52SPL ID ba371296-8731-4ffa-ab36-aff022e48d52SPL set ID 22b07167-2b7b-42ba-9ae9-cf58c98a2ab2RxCUI 477347, 602635, 642452UNII 490D9F069TUPC 0367877256900, 0367877256450, 0367877258119, 0367877257150
Pharmacologic class
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

N467877025790 followed by a unit qualifier and the quantity

Package 67877-0257-90. 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)

Lanthanum carbonate is a phosphate binder indicated to reduce serum phosphate in patients with end-stage renal disease (ESRD). Management of elevated serum phosphorus levels in patients with ESRD usually includes all of the following: reduction in dietary intake of phosphate, removal of phosphate by dialysis, and reduction of intestinal phosphate absorption with phosphate binders. Lanthanum carbonate is a phosphate binder indicated to reduce serum phosphate in patients with end-stage renal disease (ESRD). ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 67877-257

What is NDC 67877-257?
67877-257 is the product NDC for Lanthanum Carbonate, Lanthanum carbonate 750 mg/1 tablet, chewable, listed with the FDA by Ascend Laboratories, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Lanthanum Carbonate.
What is the active ingredient?
Lanthanum carbonate.
Who is the labeler?
Ascend Laboratories, LLC, NDC labeler code 67877. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Lanthanum Carbonate?
17 other product NDCs are listed under this name. See all Lanthanum Carbonate 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 Lanthanum Carbonate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Lanthanum CarbonateLanthanum carbonate 500 mg/1Tablet, ChewableOralAscend Laboratories, LLC67877-25667877-0256-90
Lanthanum CarbonateLanthanum carbonate 1000 mg/1Tablet, ChewableOralAscend Laboratories, LLC67877-25867877-0258-90
Lanthanum carbonateLanthanum carbonate 500 mg/1Tablet, ChewableOralTeva Pharmaceuticals USA, Inc.0093-593800093-5938-98
Lanthanum carbonateLanthanum carbonate 750 mg/1Tablet, ChewableOralTeva Pharmaceuticals USA, Inc.0093-593900093-5939-98
Lanthanum carbonateLanthanum carbonate 1000 mg/1Tablet, ChewableOralTeva Pharmaceuticals USA, Inc.0093-594000093-5940-98
Lanthanum carbonateLanthanum carbonate 750 mg/1Tablet, ChewableOralCipla USA Inc.69097-93569097-0935-98
Lanthanum carbonateLanthanum carbonate 500 mg/1Tablet, ChewableOralCipla USA Inc.69097-93469097-0934-98
Lanthanum carbonateLanthanum carbonate 1000 mg/1Tablet, ChewableOralCipla USA Inc.69097-93669097-0936-98
Lanthanum carbonateLanthanum carbonate 750 mg/1Tablet, ChewableOralExelan Pharmaceuticals, Inc.76282-47776282-0477-90
Lanthanum carbonateLanthanum carbonate 500 mg/1Tablet, ChewableOralExelan Pharmaceuticals, Inc.76282-47676282-0476-90

All 18 Lanthanum Carbonate NDCs

Other NDCs under ANDA 202329

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

FDA NDC Directory listings under ANDA 202329
ProductStrengthForm · routeLabelerProduct NDC
Lanthanum CarbonateLanthanum carbonate 500 mg/1Tablet, ChewableOralAscend Laboratories, LLC67877-256
Lanthanum CarbonateLanthanum carbonate 1000 mg/1Tablet, ChewableOralAscend Laboratories, LLC67877-258

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