NDC codes

FDA NDC Directory
Product NDC (as listed)43066-555Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43066-0555Add 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
43066-555-24430660555244306605552424 BAG in 1 CARTON (43066-555-24) / 50 mL in 1 BAGMarketed from Aug 27, 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

Generic name (nonproprietary)
dexmedetomidine hydrochloride in 0.9% sodium chloride
Active ingredients
Dexmedetomidine hydrochloride — 200 ug/50mL
Dosage form
Injection
Route
Intravenous
Labeler
Baxter Healthcare CompanyNDC labeler code 43066
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208532
Marketing start
Listing expires
Other FDA classes
Adrenergic alpha2-Agonists (Mechanism)General Anesthesia (Physiologic effect)
Identifiers
Product ID 43066-555_5ae6fcf6-cd01-4b89-af44-962f5452fe72SPL ID 5ae6fcf6-cd01-4b89-af44-962f5452fe72
Pharmacologic class
Central alpha-2 Adrenergic Agonist

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

N443066055524 followed by a unit qualifier and the quantity

Package 43066-0555-24. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 43066-555

What is NDC 43066-555?
43066-555 is the product NDC for Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride, Dexmedetomidine hydrochloride 200 ug/50mL injection, listed with the FDA by Baxter Healthcare Company. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride.
What is the active ingredient?
Dexmedetomidine hydrochloride.
Who is the labeler?
Baxter Healthcare Company, NDC labeler code 43066. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride?
6 other product NDCs are listed under this name. See all Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride 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 Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Dexmedetomidine Hydrochloride in 0.9% Sodium Chloridedexmedetomidine hydrochlorideDexmedetomidine hydrochloride 4 ug/mLInjection, SolutionIntravenousSagent Pharmaceuticals25021-61525021-0615-5025021-0615-51
Dexmedetomidine Hydrochloride In 0.9% Sodium ChlorideDexmedetomidine hydrochloride 4 ug/mLInjectionIntravenousSandoz Inc.0781-349300781-3493-95
Dexmedetomidine Hydrochloride In 0.9% Sodium ChlorideDexmedetomidine hydrochloride 4 ug/mLInjectionIntravenousSandoz Inc.0781-349400781-3494-95
Dexmedetomidine Hydrochloride In 0.9% Sodium ChlorideDexmedetomidine hydrochloride 4 ug/mLInjectionIntravenousSandoz Inc.0781-349500781-3495-95
Dexmedetomidine Hydrochloride In 0.9% Sodium ChlorideDexmedetomidine hydrochloride 4 ug/mLInjectionIntravenousProPharma Distribution84549-49384549-0493-95
Dexmedetomidine Hydrochloride In 0.9% Sodium ChlorideDexmedetomidine hydrochloride 400 ug/100mLInjectionIntravenousBaxter Healthcare Company43066-55743066-0557-12

Other NDCs under ANDA 208532

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

FDA NDC Directory listings under ANDA 208532
ProductStrengthForm · routeLabelerProduct NDC
Dexmedetomidine HydrochlorideDexmedetomidine hydrochloride 200 ug/50mLInjectionIntravenousBaxter Healthcare Company43066-561
Dexmedetomidine Hydrochloride In 0.9% Sodium ChlorideDexmedetomidine hydrochloride 400 ug/100mLInjectionIntravenousBaxter Healthcare Company43066-557
Dexmedetomidine HydrochlorideDexmedetomidine hydrochloride 400 ug/100mLInjectionIntravenousBaxter Healthcare Company43066-565
Dexmedetomidine HydrochlorideDexmedetomidine hydrochloride 200 ug/50mLInjectionIntravenousBaxter Healthcare Company0338-9555
Dexmedetomidine HydrochlorideDexmedetomidine hydrochloride 400 ug/100mLInjectionIntravenousBaxter Healthcare Company0338-9557

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