NDC codes

FDA NDC Directory
Product NDC (as listed)51662-1528Labeler and product segments. Claims need a package NDC.
Product NDC at billing width51662-1528Add 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
51662-1528-151662152801516621528014 mL in 1 VIAL (51662-1528-1)Marketed from Aug 8, 2021
51662-1528-3516621528035166215280310 POUCH in 1 CASE (51662-1528-3) / 1 VIAL in 1 POUCH (51662-1528-2) / 4 mL in 1 VIALMarketed from Jul 10, 2022

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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
HF Acquisition Co LLC, DBA HealthFirstNDC labeler code 51662
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 203662
Marketing start
Listing expires
Other FDA classes
Catecholamines (Chemical structure)
Identifiers
Product ID 51662-1528_54a0d021-45da-b39c-e063-6394a90a3c61SPL ID 54a0d021-45da-b39c-e063-6394a90a3c61SPL set ID c90d875c-8e6e-284e-e053-2a95a90a334fRxCUI 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

N451662152801 followed by a unit qualifier and the quantity

Package 51662-1528-01. 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)

Norepinephrine Bitartrate Injection, USP is indicated to raise blood pressure in adult patients with severe, acute hypotension.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51662-1528

What is NDC 51662-1528?
51662-1528 is the product NDC for Norepinephrine Bitartrate, Norepinephrine bitartrate 1 mg/mL injection, listed with the FDA by HF Acquisition Co LLC, DBA HealthFirst. It has 2 package NDCs, 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?
HF Acquisition Co LLC, DBA HealthFirst, NDC labeler code 51662. 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?
26 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
norepinephrine bitartrateNorepinephrine bitartrate 1 mg/mLInjection, SolutionIntravenousAvenacy, LLC83634-30783634-0307-04
norepinephrine bitartrateNorepinephrine bitartrate 1 mg/mLInjection, Solution, ConcentrateIntravenousNovadoz Pharmaceuticals LLC72205-24172205-0241-07
Norepinephrine BitartrateNorepinephrine bitartrate 1 mg/mLInjection, Solution, ConcentrateIntravenousAnthea Pharma Private Limited83854-01783854-0017-10
Norepinephrine BitartrateNorepinephrine bitartrate 1 mg/mLInjection, Solution, ConcentrateIntravenousBIOCON PHARMA INC.70377-12170377-0121-12
Norepinephrine bitartrateNorepinephrine bitartrate 1 mg/mLInjection, Solution, ConcentrateIntravenousCamber Pharmaceuticals, Inc.31722-37231722-0372-32
Norepinephrine BitartrateNorepinephrine bitartrate 1 mg/mLInjection, Solution, ConcentrateIntravenousMeitheal Pharmaceuticals Inc.71288-43971288-0439-05
Norepinephrine BitartrateNorepinephrine bitartrate 1 mg/mLInjectionIntravenousRising Pharma Holdings, Inc.64980-63064980-0630-41
Norepinephrine BitartrateNorepinephrine bitartrate 1 mg/mLInjectionIntravenousCaplin Steriles Limited65145-13365145-0133-10
Norepinephrine BitartrateNorepinephrine bitartrate 1 mg/mLInjectionIntravenousBE Pharmaceuticals Inc.71839-14371839-0143-1071839-0143-25
Norepinephrine BitartrateNorepinephrine bitartrate 1 mg/mLInjectionIntravenousNorthStar Rx LLC72603-18072603-0180-10

All 27 Norepinephrine Bitartrate NDCs

Other NDCs under ANDA 203662

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

FDA NDC Directory listings under ANDA 203662
ProductStrengthForm · routeLabelerProduct NDC
Norepinephrine BitartrateNorepinephrine bitartrate 1 mg/mLInjectionIntravenousHikma Pharmaceuticals USA Inc.0143-9318

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