NDC codes

FDA NDC Directory
Product NDC (as listed)60505-6270Labeler and product segments. Claims need a package NDC.
Product NDC at billing width60505-6270Add 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
60505-6270-160505627001605056270011 KIT in 1 CARTON (60505-6270-1) * 1 mL in 1 VIAL, GLASS (60505-6281-0) * 1 mL in 1 SYRINGE, GLASS (60505-6276-0)Marketed from May 13, 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)
Cetrorelix acetate
Generic name (nonproprietary)
cetrorelix acetate for injection
Dosage form
Kit
Route
Subcutaneous
Labeler
Apotex Corp.NDC labeler code 60505
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 217776
Marketing start
Listing expires
Identifiers
Product ID 60505-6270_944e22b5-4cab-4aa7-955c-d6bdecb7f716SPL ID 944e22b5-4cab-4aa7-955c-d6bdecb7f716SPL set ID 95b852d6-26a4-4aaf-a4c3-26340a24723dRxCUI 283402

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

N460505627001 followed by a unit qualifier and the quantity

Package 60505-6270-01. 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 Cetrorelix Acetate for Injection is indicated for the inhibition of premature LH surges in women undergoing controlled ovarian stimulation.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 60505-6270

What is NDC 60505-6270?
60505-6270 is the product NDC for Cetrorelix acetate (cetrorelix acetate for injection) kit, listed with the FDA by Apotex Corp.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Cetrorelix acetate (Cetrorelix Acetate for Injection).
Who is the labeler?
Apotex Corp., NDC labeler code 60505. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cetrorelix acetate?
4 other product NDCs are listed under this name. See all Cetrorelix 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 Cetrorelix acetate NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
cetrorelix acetate—KitFRESENIUS KABI USA, LLC65219-29265219-0292-77
cetrorelix acetate—KitGland Pharma Limited68083-60068083-0600-01
Cetrorelix Acetate—KitSubcutaneousMeitheal Pharmaceuticals Inc.71288-55871288-0558-90
Cetrorelix acetatecetrorelix acetate for injection—KitSubcutaneousQilu Pharmaceutical Co., Ltd.67184-060567184-0605-02

Other NDCs under ANDA 217776

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

FDA NDC Directory listings under ANDA 217776
ProductStrengthForm · routeLabelerProduct NDC
Cetrorelix acetatecetrorelix acetate for injection—KitSubcutaneousQilu Pharmaceutical Co., Ltd.67184-0605

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