NDC codes

FDA NDC Directory
Product NDC (as listed)81298-9659Labeler and product segments. Claims need a package NDC.
Product NDC at billing width81298-9659Add 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
81298-9659-38129896590310 POUCH in 1 BOX (81298-9659-3) / 1 BAG in 1 POUCH (81298-9659-1) / 250 mL in 1 BAGMarketed from Feb 2, 2024

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
Generic name (nonproprietary)
norepinephrine bitartrate
Active ingredients
Norepinephrine bitartrate — 16 ug/mL
Dosage form
Solution
Route
Intravenous
Labeler
Long Grove Pharmaceuticals, LLCNDC labeler code 81298
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 214628
Marketing start
Listing expires
Other FDA classes
Catecholamines (Chemical structure)
Identifiers
Product ID 81298-9659_329c5273-4dc5-4738-bf21-660e73d91eb9SPL ID 329c5273-4dc5-4738-bf21-660e73d91eb9SPL set ID 759807dd-61a8-4f6f-8bf5-f6ee773c81bcRxCUI 2475337, 2475340, 2619579UNII 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

N481298965903 followed by a unit qualifier and the quantity

Package 81298-9659-03. 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)

Norepinephrine in Sodium Chloride Injection is indicated to raise blood pressure in adult patients with severe, acute hypotension. Norepinephrine in Sodium Chloride 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 81298-9659

What is NDC 81298-9659?
81298-9659 is the product NDC for Norepinephrine (norepinephrine bitartrate), Norepinephrine bitartrate 16 ug/mL solution, listed with the FDA by Long Grove Pharmaceuticals, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Norepinephrine (Norepinephrine Bitartrate).
What is the active ingredient?
Norepinephrine bitartrate.
Who is the labeler?
Long Grove Pharmaceuticals, LLC, NDC labeler code 81298. 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?
5 other product NDCs are listed under this name. See all Norepinephrine 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 NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Norepinephrinenorepinephrine bitartrateNorepinephrine bitartrate 32 ug/mLSolutionIntravenousLong Grove Pharmaceuticals, LLC81298-965581298-9655-03
Norepinephrinenorepinephrine bitartrateNorepinephrine bitartrate 64 ug/mLSolutionIntravenousLong Grove Pharmaceuticals, LLC81298-965881298-9658-03
Norepinephrinenorepinephrine (bitartrate)Norepinephrine bitartrate 8 [hp_X]/mLLiquidOralDeseret Biologicals, Inc.43742-148943742-1489-01
NorepinephrineNorepinephrine 6 [hp_X]/mLLiquidOralBioActive Nutritional, Inc.43857-026043857-0260-01
NorepinephrineNorepinephrine 6 [hp_X]/mLLiquidOralBioActive Nutritional, Inc.43857-016143857-0161-01

Other NDCs under NDA 214628

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

FDA NDC Directory listings under NDA 214628
ProductStrengthForm · routeLabelerProduct NDC
Norepinephrinenorepinephrine bitartrateNorepinephrine bitartrate 32 ug/mLSolutionIntravenousLong Grove Pharmaceuticals, LLC81298-9655
Norepinephrinenorepinephrine bitartrateNorepinephrine bitartrate 64 ug/mLSolutionIntravenousLong Grove Pharmaceuticals, LLC81298-9658

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