NDC codes

FDA NDC Directory
Product NDC (as listed)76297-006Labeler and product segments. Claims need a package NDC.
Product NDC at billing width76297-0006Add 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
76297-006-03762970006037629700060330 BAG in 1 CARTON (76297-006-03) / 250 mL in 1 BAG (76297-006-02)Marketed from Oct 25, 2019
76297-006-04762970006047629700060439 BAG in 1 CARTON (76297-006-04) / 250 mL in 1 BAG (76297-006-02)Marketed from Oct 25, 2019

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)
Anticoagulant Sodium Citrate
Generic name (nonproprietary)
trisodium citrate dihydrate
Active ingredients
Trisodium citrate dihydrate — 40 mg/mL
Dosage form
Solution
Route
Extracorporeal
Labeler
LABORATORIOS GRIFOLS SANDC labeler code 76297
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application BA 125697
Marketing start
Listing expires
Other FDA classes
Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)
Identifiers
Product ID 76297-006_fa83d193-9cfc-40c0-b924-b1685c50d08aSPL ID fa83d193-9cfc-40c0-b924-b1685c50d08aSPL set ID db8334be-5b8b-4811-811a-efbe32b6d147UNII B22547B95K
Pharmacologic class
Anti-coagulant; Calculi Dissolution Agent

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

NDC on a medical claim

N476297000603 followed by a unit qualifier and the quantity

Package 76297-0006-03. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 76297-006

What is NDC 76297-006?
76297-006 is the product NDC for Anticoagulant Sodium Citrate (trisodium citrate dihydrate), Trisodium citrate dihydrate 40 mg/mL solution, listed with the FDA by LABORATORIOS GRIFOLS SA. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Anticoagulant Sodium Citrate (Trisodium Citrate Dihydrate).
What is the active ingredient?
Trisodium citrate dihydrate.
Who is the labeler?
LABORATORIOS GRIFOLS SA, NDC labeler code 76297. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Anticoagulant Sodium Citrate?
1 other product NDC are listed under this name. See all Anticoagulant Sodium Citrate 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 Anticoagulant Sodium Citrate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Anticoagulant Sodium Citratetrisodium citrate dihydrateTrisodium citrate dihydrate 40 mg/mLSolutionExtracorporealBaxter Healthcare Corporation0338-966900338-9669-01

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