What is NDC 43066-997?

43066-997 is the product NDC for Norepinephrine Bitartrate, Norepinephrine bitartrate 1 mg/mL injection, listed with the FDA by Baxter Healthcare Company. It has 1 package NDC, shown above in 10- and 11-digit form.

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 Norepinephrine Bitartrate?

27 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Norepinephrine Bitartrate NDC 43066-997

NDC codes

FDA NDC Directory

Product NDC (as listed)43066-997Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43066-0997Add 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 NDC	11-digit (billing)	Package	Copy
43066-997-10	43066099710	10 VIAL, SINGLE-DOSE in 1 CARTON (43066-997-10) / 4 mL in 1 VIAL, SINGLE-DOSE (43066-997-01)Marketed from May 6, 2021

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): Norepinephrine Bitartrate
Generic name (nonproprietary): norepinephrine bitartrate
Active ingredients: Norepinephrine bitartrate — 1 mg/mL
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 214323
Marketing start: May 6, 2021
Listing expires: Dec 31, 2027
Other FDA classes: Catecholamines (Chemical structure)
Identifiers: Product ID 43066-997_214d6f15-f128-4815-bb82-f9abf88aff24SPL ID 214d6f15-f128-4815-bb82-f9abf88aff24SPL set ID e375a0b9-4d26-4749-bbc3-43d63a7cf65aRxCUI 242969UNII IFY5PE3ZRW
Pharmacologic class: Catecholamine

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

N443066099710 followed by a unit qualifier and the quantity

Package 43066-0997-10. 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 May 6, 2021.

Indications (excerpt from the label)

Norepinephrine Bitartrate Injection is indicated to raise blood pressure in adult patients with severe, acute hypotension. Norepinephrine Bitartrate Injection is a catecholamine indicated for restoration of blood pressure in adult patients with acute hypotensive states. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43066-997

What is NDC 43066-997?: 43066-997 is the product NDC for Norepinephrine Bitartrate, Norepinephrine bitartrate 1 mg/mL 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?: Norepinephrine Bitartrate.
What is the active ingredient?: Norepinephrine bitartrate.
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 Norepinephrine Bitartrate?: 27 other product NDCs are listed under this name. See all Norepinephrine Bitartrate 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 Norepinephrine Bitartrate NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
norepinephrine bitartrate	Norepinephrine bitartrate 1 mg/mL	Injection, SolutionIntravenous	Avenacy, LLC	83634-307	83634-0307-04
norepinephrine bitartrate	Norepinephrine bitartrate 1 mg/mL	Injection, Solution, ConcentrateIntravenous	Novadoz Pharmaceuticals LLC	72205-241	72205-0241-07
Norepinephrine Bitartrate	Norepinephrine bitartrate 1 mg/mL	Injection, Solution, ConcentrateIntravenous	Anthea Pharma Private Limited	83854-017	83854-0017-10
Norepinephrine Bitartrate	Norepinephrine bitartrate 1 mg/mL	Injection, Solution, ConcentrateIntravenous	BIOCON PHARMA INC.	70377-121	70377-0121-12
Norepinephrine bitartrate	Norepinephrine bitartrate 1 mg/mL	Injection, Solution, ConcentrateIntravenous	Camber Pharmaceuticals, Inc.	31722-372	31722-0372-32
Norepinephrine Bitartrate	Norepinephrine bitartrate 1 mg/mL	Injection, Solution, ConcentrateIntravenous	Meitheal Pharmaceuticals Inc.	71288-439	71288-0439-05
Norepinephrine Bitartrate	Norepinephrine bitartrate 1 mg/mL	InjectionIntravenous	Rising Pharma Holdings, Inc.	64980-630	64980-0630-41
Norepinephrine Bitartrate	Norepinephrine bitartrate 1 mg/mL	InjectionIntravenous	Caplin Steriles Limited	65145-133	65145-0133-10
Norepinephrine Bitartrate	Norepinephrine bitartrate 1 mg/mL	InjectionIntravenous	BE Pharmaceuticals Inc.	71839-143	71839-0143-1071839-0143-25
Norepinephrine Bitartrate	Norepinephrine bitartrate 1 mg/mL	InjectionIntravenous	NorthStar Rx LLC	72603-180	72603-0180-10

All 28 Norepinephrine Bitartrate NDCs

Other NDCs under ANDA 214323

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

FDA NDC Directory listings under ANDA 214323
Product	Strength	Form · route	Labeler	Product NDC
Norepinephrine Bitartrate	Norepinephrine bitartrate 1 mg/mL	Injection, SolutionIntravenous	Sagent Pharmaceuticals	25021-316
Norepinephrine bitartrate	Norepinephrine bitartrate 1 mg/mL	InjectionIntravenous	Gland Pharma Limited	68083-437