NDC codes

FDA NDC Directory
Product NDC (as listed)70511-162Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70511-0162Add 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
70511-162-0270511016202705110162021 INJECTION in 1 VIAL, SINGLE-DOSE (70511-162-02)Marketed from Aug 11, 2022

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)
Bortezomib
Generic name (nonproprietary)
bortezomib
Active ingredients
Bortezomib — 2.5 mg/1
Dosage form
Injection
Route
Intravenous
Labeler
MAIA Pharmaceuticals, Inc.NDC labeler code 70511
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 215331
Marketing start
Listing expires
Other FDA classes
Proteasome Inhibitors (Mechanism)
Identifiers
Product ID 70511-162_2cc294fe-75e3-4ed9-8259-c6e5bc5e8286SPL ID 2cc294fe-75e3-4ed9-8259-c6e5bc5e8286SPL set ID c40e6a28-d577-43d4-bca6-bef28da1d580RxCUI 2608948, 2608952UNII 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

N470511016202 followed by a unit qualifier and the quantity

Package 70511-0162-02. 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)

Bortezomib injection is a proteasome inhibitor indicated for: treatment of adult patients with multiple myeloma (1.1) treatment of adult patients with mantle cell lymphoma (1.2) 1.1 Multiple Myeloma Bortezomib Injection is indicated for the treatment of adult patients with multiple myeloma. 1.2 Mantle Cell Lymphoma Bortezomib Injection is indicated for the treatment of adult patients with mantle cell lymphoma.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70511-162

What is NDC 70511-162?
70511-162 is the product NDC for Bortezomib, Bortezomib 2.5 mg/1 injection, listed with the FDA by MAIA Pharmaceuticals, Inc.. 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?
MAIA Pharmaceuticals, Inc., NDC labeler code 70511. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
BortezomibBortezomib 3.5 mg/1Injection, Powder, Lyophilized, For solutionIntravenous, SubcutaneousAvenacy, LLC83634-20883634-0208-10
BortezomibBortezomib 1 mg/1Injection, Powder, Lyophilized, For solutionIntravenous, SubcutaneousGland Pharma Limited68083-65068083-0650-01
BortezomibBortezomib 2.5 mg/1Injection, Powder, Lyophilized, For solutionIntravenous, SubcutaneousGland Pharma Limited68083-65168083-0651-01
BortezomibBortezomib 3.5 mg/1Injection, Powder, Lyophilized, For solutionIntravenous, SubcutaneousNingbo Shuangcheng Pharmaceutical Co., Ltd.75007-50175007-0501-3175007-0501-32
BortezomibBortezomib 3.5 mg/1Injection, Powder, Lyophilized, For solutionIntravenous, SubcutaneousSagent Pharmaceuticals25021-26225021-0262-10
BortezomibBortezomib 3.5 mg/3.5mLInjection, Powder, Lyophilized, For solutionIntravenous, SubcutaneousSomerset Therapeutics LLC70069-83670069-0836-01
BortezomibBortezomib 3.5 mg/1Injection, Powder, Lyophilized, For solutionIntravenous, SubcutaneousNorthStar RxLLC72603-27072603-0270-01
BortezomibBortezomib 3.5 mg/1.4mLInjectionIntravenous, SubcutaneousShilpa Medicare Limited63759-303263759-3032-01
BortezomibBortezomib 3.5 mg/1Injection, Powder, Lyophilized, For solutionIntravenous, SubcutaneousCamber Pharmaceuticals, Inc.31722-30331722-0303-31
BortezomibBortezomib 3.5 mg/3.5mLInjection, Powder, Lyophilized, For solutionIntravenous, SubcutaneousSintetica US LLC83090-00883090-0008-01

All 30 Bortezomib NDCs

Other NDCs under NDA 215331

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

FDA NDC Directory listings under NDA 215331
ProductStrengthForm · routeLabelerProduct NDC
BortezomibBortezomib 1 mg/1InjectionIntravenousMAIA Pharmaceuticals, Inc.70511-161

Free account

Log in to keep searching

You’ve used your 3 free searches. Med-Code is free: log in or create a free profile to keep looking up NDCs, J-codes and drugs.

Create a free profileLog in