NDC codes

FDA NDC Directory
Product NDC (as listed)68083-472Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68083-0472Add 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
68083-472-0168083047201680830472011 BLISTER PACK in 1 CARTON (68083-472-01) / 1 SYRINGE, GLASS in 1 BLISTER PACK / 1 mL in 1 SYRINGE, GLASSMarketed from Feb 28, 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

Brand name (proprietary)
Ganirelix Acetate
Generic name (nonproprietary)
ganirelix acetate
Active ingredients
Ganirelix acetate — 250 ug/.5mL
Dosage form
Injection, Solution
Route
Subcutaneous
Labeler
Gland Pharma LimitedNDC labeler code 68083
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 215658
Marketing start
Listing expires
Other FDA classes
Decreased GnRH Secretion (Physiologic effect)Gonadotropin Releasing Hormone Receptor Antagonists (Mechanism)
Identifiers
Product ID 68083-472_9d647fa7-adc3-4767-a8e5-1b44b07cdd34SPL ID 9d647fa7-adc3-4767-a8e5-1b44b07cdd34SPL set ID cad7c09c-234b-4e73-b460-a1b1f7adc28dRxCUI 855200UNII 56U7906FQWUPC 0368083472016
Pharmacologic class
Gonadotropin Releasing Hormone Receptor Antagonist

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

N468083047201 followed by a unit qualifier and the quantity

Package 68083-0472-01. 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)

INDICATIONS AND USAGE Ganirelix Acetate Injection is indicated for the inhibition of premature LH surges in women undergoing controlled ovarian hyperstimulation.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68083-472

What is NDC 68083-472?
68083-472 is the product NDC for Ganirelix Acetate, Ganirelix acetate 250 ug/.5mL injection, solution, listed with the FDA by Gland Pharma Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ganirelix Acetate.
What is the active ingredient?
Ganirelix acetate.
Who is the labeler?
Gland Pharma Limited, NDC labeler code 68083. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ganirelix Acetate?
8 other product NDCs are listed under this name. See all Ganirelix Acetate 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 Ganirelix Acetate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Ganirelix AcetateGanirelix acetate 250 ug/.5mLInjection, SolutionSubcutaneousMullan Pharmaceutical Inc.83301-008283301-0082-01
Ganirelix AcetateGanirelix acetate 250 ug/.5mLInjection, SolutionSubcutaneousQilu Pharmaceutical Co., Ltd.67184-057467184-0574-01
Ganirelix AcetateGanirelix acetate 250 ug/.5mLInjectionSubcutaneousXiromed LLC70700-32770700-0327-98
Ganirelix AcetateGanirelix acetate 250 ug/.5mLInjection, SolutionSubcutaneousLupin Pharmaceuticals, Inc.70748-27470748-0274-01
Ganirelix AcetateGanirelix acetate 250 ug/.5mLInjectionSubcutaneousFresenius Kabi USA, LLC65219-02865219-0028-05
Ganirelix AcetateGanirelix acetate 250 ug/.5mLInjectionSubcutaneousAmphastar Pharmaceuticals, Inc.0548-500100548-5001-00
Ganirelix AcetateGanirelix acetate 250 ug/.5mLInjection, SolutionSubcutaneousMeitheal Pharmaceuticals Inc.71288-55471288-0554-80
Ganirelix AcetateGanirelix acetate 250 ug/.5mLInjection, SolutionSubcutaneousOrganon LLC78206-13878206-0138-02

Other NDCs under ANDA 215658

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

FDA NDC Directory listings under ANDA 215658
ProductStrengthForm · routeLabelerProduct NDC
Ganirelix AcetateGanirelix acetate 250 ug/.5mLInjectionSubcutaneousFresenius Kabi USA, LLC65219-028
Ganirelix AcetateGanirelix acetate 250 ug/.5mLInjectionSubcutaneousXiromed LLC70700-327

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