Plerixafor NDC 70771-1776

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 NDC	11-digit (billing)	Package	Copy
70771-1776-1	70771177601	1 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 Limited
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 208980
Marketing start: Jul 28, 2023
Listing expires: Dec 31, 2026
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 Jul 28, 2023.

Full label on DailyMed (opens in a new tab)

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
Product	Strength	Form · route	Labeler	Product NDC
Plerixafor	Plerixafor 24 mg/1.2mL	InjectionSubcutaneous	Zydus Pharmaceuticals USA Inc.	70710-1208