NDC codes

FDA NDC Directory
Product NDC (as listed)70771-1776Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70771-1776Add 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
70771-1776-1707711776011 VIAL, SINGLE-USE in 1 CARTON (70771-1776-1) / 1.2 mL in 1 VIAL, SINGLE-USEMarketed from Jul 28, 2023

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)
Plerixafor
Generic name (nonproprietary)
plerixafor
Active ingredients
Plerixafor — 24 mg/1.2mL
Dosage form
Injection
Route
Subcutaneous
Labeler
Zydus Lifesciences LimitedNDC labeler code 70771
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 208980
Marketing start
Listing expires
Other FDA classes
Increased Hematopoietic Stem Cell Mobilization (Physiologic effect)
Identifiers
Product ID 70771-1776_41b76e97-b780-4fc8-b073-13bf155ad8a5SPL ID 41b76e97-b780-4fc8-b073-13bf155ad8a5SPL set ID 43df348a-d7f2-4f14-8131-c916679a98ebRxCUI 828700UNII S915P5499N
Pharmacologic class
Hematopoietic Stem Cell Mobilizer

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

N470771177601 followed by a unit qualifier and the quantity

Package 70771-1776-01. 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 .

Full label on DailyMed (opens in a new tab)

About NDC 70771-1776

What is NDC 70771-1776?
70771-1776 is the product NDC for Plerixafor, Plerixafor 24 mg/1.2mL injection, listed with the FDA by Zydus Lifesciences Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Plerixafor.
What is the active ingredient?
Plerixafor.
Who is the labeler?
Zydus Lifesciences Limited, NDC labeler code 70771. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Plerixafor?
11 other product NDCs are listed under this name. See all Plerixafor 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 Plerixafor NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
PlerixaforPlerixafor 24 mg/1.2mLInjection, SolutionSubcutaneousCamber Pharmaceuticals, Inc.31722-37331722-0373-31
PlerixaforPlerixafor 20 mg/mLInjection, SolutionSubcutaneousSagent Pharmaceuticals25021-41625021-0416-01
PlerixaforPlerixafor 24 mg/1.2mLInjection, SolutionSubcutaneousGland Pharma Limited68083-15568083-0155-01
PlerixaforPlerixafor 24 mg/1.2mLSolutionSubcutaneousDr. Reddy's Laboratories Inc43598-30843598-0308-23
PlerixaforPlerixafor 24 mg/1.2mLInjectionSubcutaneousZydus Pharmaceuticals USA Inc.70710-120870710-1208-01
plerixaforPlerixafor 24 mg/1.2mLInjection, SolutionSubcutaneousAmneal Pharmaceuticals LLC70121-169470121-1694-02
PlerixaforPlerixafor 24 mg/1.2mLInjection, SolutionSubcutaneousBryant Ranch Prepack72162-264272162-2642-02
PlerixaforPlerixafor 24 mg/1.2mLInjection, SolutionSubcutaneousNovadoz Pharmaceuticals LLC72205-24972205-0249-01
PlerixaforPlerixafor 24 mg/1.2mLSolutionSubcutaneousEugia US LLC55150-35655150-0356-01
PlerixaforPlerixafor 24 mg/1.2mLSolutionSubcutaneousMeitheal Pharmaceuticals Inc.71288-15571288-0155-01

All 12 Plerixafor NDCs

Other NDCs under ANDA 208980

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

FDA NDC Directory listings under ANDA 208980
ProductStrengthForm · routeLabelerProduct NDC
PlerixaforPlerixafor 24 mg/1.2mLInjectionSubcutaneousZydus Pharmaceuticals USA Inc.70710-1208

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