NDC codes

FDA NDC Directory
Product NDC (as listed)14537-820Labeler and product segments. Claims need a package NDC.
Product NDC at billing width14537-0820Add 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
14537-820-03145370820031453708200350 POUCH in 1 CASE (14537-820-03) / 1 BAG in 1 POUCH (14537-820-01) / 50 mL in 1 BAG (14537-820-00)Marketed from Jul 18, 2023

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

Generic name (nonproprietary)
dextrose monohydrate, sodium citrate, unspecified form, and citric acid monohydrate
Active ingredients
Dextrose monohydrate — .245 g/10mLSodium citrate, Unspecified form — .22 g/10mLCitric acid monohydrate — .08 g/10mL
Dosage form
Solution
Route
Intravenous
Labeler
Terumo BCT, LtdNDC labeler code 14537
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application BA 110057
Marketing start
Listing expires
Other FDA classes
Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)
Identifiers
Product ID 14537-820_73126eb8-5fba-4a43-b84a-057382d4f0f4SPL ID 73126eb8-5fba-4a43-b84a-057382d4f0f4SPL set ID 0130d7c8-d067-4528-beb7-166559c33be9UNII LX22YL083G, 1Q73Q2JULR, 2968PHW8QP
Pharmacologic class
Anti-coagulant; Calculi Dissolution Agent; Osmotic Laxative

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.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N414537082003 followed by a unit qualifier and the quantity

Package 14537-0820-03. 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 .

Indications (excerpt from the label)

ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A is an anticoagulant intended for use only with devices that prepare Platelet Rich Plasma (PRP) products for extracorporeal use. [See Dosage and Administration (2) .] ANTICOAGULANT CITRATE DEXTROSE SOLUTION USP (ACD) SOLUTION A is an anticoagulant intended for use only with devices that prepare Platelet Rich Plasma (PRP) products for extracorporeal use. See the device operator's manual for additional information and complete usage instructions. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 14537-820

What is NDC 14537-820?
14537-820 is the product NDC for Anticoagulant Citrate Dextrose (ACD-A), Dextrose monohydrate .245 g/10mL + 2 more ingredients solution, listed with the FDA by Terumo BCT, Ltd. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Anticoagulant Citrate Dextrose (ACD-A) (Dextrose Monohydrate, sodium citrate, unspecified form, and Citric Acid Monohydrate).
What is the active ingredient?
Dextrose monohydrate, Sodium citrate, Unspecified form, Citric acid monohydrate.
Who is the labeler?
Terumo BCT, Ltd, NDC labeler code 14537. 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 Citrate Dextrose (ACD-A)?
None: this is the only finished product listed under this name.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other NDCs under BA 110057

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

FDA NDC Directory listings under BA 110057
ProductStrengthForm · routeLabelerProduct NDC
Anticoagulant Citrate Dextrose A ACD-ACitric acid monohydrate .08 g/10mL + 2 more ingredientsInjection, SolutionExtracorporealArteriocyte Medical Systems, Inc.43203-852

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