NDC codes

FDA NDC Directory
Product NDC (as listed)68083-171Labeler and product segments. Claims need a package NDC.
Product NDC at billing width68083-0171Add 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
68083-171-01680830171016808301710120 mL in 1 VIAL (68083-171-01)Marketed from May 29, 2017

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)
Oxaliplatin
Generic name (nonproprietary)
oxaliplatin
Active ingredients
Oxaliplatin — 100 mg/20mL
Dosage form
Injection, Powder, Lyophilized, For solution
Route
Intravenous
Labeler
Gland Pharma LimitedNDC labeler code 68083
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 207385
Marketing start
Listing expires
Other FDA classes
Platinum-containing Compounds (EXT)
Identifiers
Product ID 68083-171_0d039035-85d1-40d4-8ee6-540026ab7a5cSPL ID 0d039035-85d1-40d4-8ee6-540026ab7a5cSPL set ID d6178bc6-9dae-413f-8f47-de75d576c5b8RxCUI 1736784, 1736786UNII 04ZR38536JUPC 0368083171018, 0368083170011
Pharmacologic class
Platinum-based Drug

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

N468083017101 followed by a unit qualifier and the quantity

Package 68083-0171-01. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

Oxaliplatin for injection USP, used in combination with infusional 5-fluorouracil/leucovorin, is indicated for: - adjuvant treatment of stage III colon cancer in patients who have undergone complete resection of the primary tumor. - treatment of advanced colorectal cancer. Oxaliplatin for injection USP is a platinum-based drug used in combination with infusional 5-fluorouracil/leucovorin, which is indicated for: - adjuvant treatment of stage III colon cancer in patients who have undergone complete resection of the primary tumor. - treatment of advanced colorectal cancer. (1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 68083-171

What is NDC 68083-171?
68083-171 is the product NDC for Oxaliplatin, Oxaliplatin 100 mg/20mL injection, powder, lyophilized, for 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?
Oxaliplatin.
What is the active ingredient?
Oxaliplatin.
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 Oxaliplatin?
39 other product NDCs are listed under this name. See all Oxaliplatin 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 Oxaliplatin NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
oxaliplatinOxaliplatin 5 mg/mLInjection, SolutionIntravenousShandong New Time Pharmaceutical Co., Ltd.42677-33642677-0336-10
oxaliplatinOxaliplatin 5 mg/mLInjection, SolutionIntravenousShandong New Time Pharmaceutical Co., Ltd.42677-33742677-0337-10
OxaliplatinOxaliplatin 50 mg/10mLInjection, Solution, ConcentrateIntravenousCamber Pharmaceuticals, Inc.31722-35731722-0357-10
OxaliplatinOxaliplatin 100 mg/20mLInjection, Solution, ConcentrateIntravenousCamber Pharmaceuticals, Inc.31722-35831722-0358-20
OxaliplatinOxaliplatin 5 mg/mLInjection, SolutionIntravenousApotex Corp.60505-628760505-6287-0260505-6287-04
OxaliplatinOxaliplatin 5 mg/mLInjection, SolutionIntravenousMeitheal Pharmaceuticals Inc.71288-17171288-0171-11
OxaliplatinOxaliplatin 5 mg/mLInjection, SolutionIntravenousMeitheal Pharmaceuticals Inc.71288-17271288-0172-21
OxaliplatinOxaliplatin 5 mg/mLInjection, SolutionIntravenousNorthstar Rx LLC72603-32072603-0320-01
OxaliplatinOxaliplatin 5 mg/mLInjection, SolutionIntravenousNorthstar Rx LLC72603-42072603-0420-01
OxaliplatinOxaliplatin 5 mg/mLInjection, SolutionIntravenousBluePoint Laboratories68001-46868001-0468-3668001-0468-37

All 40 Oxaliplatin NDCs

Other NDCs under ANDA 207385

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

FDA NDC Directory listings under ANDA 207385
ProductStrengthForm · routeLabelerProduct NDC
OxaliplatinOxaliplatin 50 mg/10mLInjection, Powder, Lyophilized, For solutionIntravenousGland Pharma Limited68083-170

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