What is NDC 70771-1708?

70771-1708 is the product NDC for Bortezomib, Bortezomib 1 mg/mL injection, powder, lyophilized, for solution, listed with the FDA by Zydus Lifesciences Limited. It has 1 package NDC, shown above in 10- and 11-digit form.

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 Bortezomib?

29 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Bortezomib NDC 70771-1708 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70771-1708Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70771-1708Add 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
70771-1708-1	7077117080170771170801	1 VIAL, SINGLE-DOSE in 1 CARTON (70771-1708-1) / 3.5 mL in 1 VIAL, SINGLE-DOSEMarketed from May 2, 2022

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): Bortezomib
Generic name (nonproprietary): bortezomib
Active ingredients: Bortezomib — 1 mg/mL
Dosage form: Injection, Powder, Lyophilized, For solution
Route: Intravenous, Subcutaneous
Labeler: Zydus Lifesciences LimitedNDC labeler code 70771
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 210204
Marketing start: May 2, 2022
Listing expires: Dec 31, 2026
Other FDA classes: Proteasome Inhibitors (Mechanism)
Identifiers: Product ID 70771-1708_a7ff2205-566b-4fb5-8f33-bf73377ee093SPL ID a7ff2205-566b-4fb5-8f33-bf73377ee093SPL set ID 582c7c0d-fa25-4586-8157-a1e2653d72d9RxCUI 402243UNII 69G8BD63PP
Pharmacologic class: Proteasome Inhibitor

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

N470771170801 followed by a unit qualifier and the quantity

Package 70771-1708-01. 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 May 5, 2022.

Full label on DailyMed (opens in a new tab)

About NDC 70771-1708

What is NDC 70771-1708?: 70771-1708 is the product NDC for Bortezomib, Bortezomib 1 mg/mL injection, powder, lyophilized, for solution, 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?: Bortezomib.
What is the active ingredient?: Bortezomib.
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 Bortezomib?: 29 other product NDCs are listed under this name. See all Bortezomib 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 Bortezomib NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Bortezomib	Bortezomib 3.5 mg/1	Injection, Powder, Lyophilized, For solutionIntravenous, Subcutaneous	Avenacy, LLC	83634-208	83634-0208-10
Bortezomib	Bortezomib 1 mg/1	Injection, Powder, Lyophilized, For solutionIntravenous, Subcutaneous	Gland Pharma Limited	68083-650	68083-0650-01
Bortezomib	Bortezomib 2.5 mg/1	Injection, Powder, Lyophilized, For solutionIntravenous, Subcutaneous	Gland Pharma Limited	68083-651	68083-0651-01
Bortezomib	Bortezomib 3.5 mg/1	Injection, Powder, Lyophilized, For solutionIntravenous, Subcutaneous	Ningbo Shuangcheng Pharmaceutical Co., Ltd.	75007-501	75007-0501-3175007-0501-32
Bortezomib	Bortezomib 3.5 mg/1	Injection, Powder, Lyophilized, For solutionIntravenous, Subcutaneous	Sagent Pharmaceuticals	25021-262	25021-0262-10
Bortezomib	Bortezomib 3.5 mg/3.5mL	Injection, Powder, Lyophilized, For solutionIntravenous, Subcutaneous	Somerset Therapeutics LLC	70069-836	70069-0836-01
Bortezomib	Bortezomib 3.5 mg/1	Injection, Powder, Lyophilized, For solutionIntravenous, Subcutaneous	NorthStar RxLLC	72603-270	72603-0270-01
Bortezomib	Bortezomib 3.5 mg/1.4mL	InjectionIntravenous, Subcutaneous	Shilpa Medicare Limited	63759-3032	63759-3032-01
Bortezomib	Bortezomib 3.5 mg/1	Injection, Powder, Lyophilized, For solutionIntravenous, Subcutaneous	Camber Pharmaceuticals, Inc.	31722-303	31722-0303-31
Bortezomib	Bortezomib 3.5 mg/3.5mL	Injection, Powder, Lyophilized, For solutionIntravenous, Subcutaneous	Sintetica US LLC	83090-008	83090-0008-01

All 30 Bortezomib NDCs

Other NDCs under ANDA 210204

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

FDA NDC Directory listings under ANDA 210204
Product	Strength	Form · route	Labeler	Product NDC
Bortezomib	Bortezomib 1 mg/mL	Injection, Powder, Lyophilized, For solutionIntravenous, Subcutaneous	Zydus Pharmaceuticals USA Inc.	70710-1411