What is NDC 70710-2066?

70710-2066 is the product NDC for gadobutrol, Gadobutrol 604.72 mg/mL injection, listed with the FDA by Zydus Pharmaceuticals USA Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Zydus Pharmaceuticals USA Inc., NDC labeler code 70710. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for gadobutrol?

16 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

gadobutrol NDC 70710-2066 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)70710-2066Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70710-2066Add 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
70710-2066-6	70710206606	10 VIAL, SINGLE-DOSE in 1 CARTON (70710-2066-6) / 15 mL in 1 VIAL, SINGLE-DOSE (70710-2066-1)Marketed from Jul 14, 2026

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): gadobutrol
Generic name (nonproprietary): gadobutrol
Active ingredients: Gadobutrol — 604.72 mg/mL
Dosage form: Injection
Route: Intravenous
Labeler: Zydus Pharmaceuticals USA Inc.NDC labeler code 70710
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 219287
Marketing start: Jul 14, 2026
Listing expires: Dec 31, 2027
Other FDA classes: Magnetic Resonance Contrast Activity (Mechanism)
Identifiers: Product ID 70710-2066_4bdf7135-c236-4892-96e0-db2d78d53853SPL ID 4bdf7135-c236-4892-96e0-db2d78d53853SPL set ID 4ea8ae43-22ca-40c0-be72-c91a321cafd1UNII 1BJ477IO2LUPC 0370710206512, 0370710206611, 0370710206413
Pharmacologic class: Gadolinium-based Contrast Agent

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

N470710206606 followed by a unit qualifier and the quantity

Package 70710-2066-06. 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 23, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Gadobutrol Injection is indicated for: Magnetic resonance imaging (MRI) of the central nervous system (CNS) to detect and visualize areas with disrupted blood brain barrier and/or abnormal vascularity in adult and pediatric patients including term neonates MRI of the breast to assess the presence and extent of malignant breast disease in adult patients Magnetic resonance angiography (MRA) to evaluate known or suspected supra-aortic or renal artery disease in adult and pediatric patients including term neonates Cardiac MRI (CMRI) to assess myocardial perfusion (stress, rest) and late gadolinium enhancement in adult patients with known or suspected coronary artery disease (CAD) Gadobutrol Inje…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70710-2066

What is NDC 70710-2066?: 70710-2066 is the product NDC for gadobutrol, Gadobutrol 604.72 mg/mL injection, listed with the FDA by Zydus Pharmaceuticals USA Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: gadobutrol.
What is the active ingredient?: Gadobutrol.
Who is the labeler?: Zydus Pharmaceuticals USA Inc., NDC labeler code 70710. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for gadobutrol?: 16 other product NDCs are listed under this name. See all gadobutrol 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 gadobutrol NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Zydus Pharmaceuticals USA Inc.	70710-2064	70710-2064-06
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Zydus Pharmaceuticals USA Inc.	70710-2065	70710-2065-06
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Viwit Pharmaceutical Co., Ltd.	42337-006	42337-0006-02
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Viwit Pharmaceutical Co., Ltd.	42337-005	42337-0005-02
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Viwit Pharmaceutical Co., Ltd.	42337-007	42337-0007-02
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Slate Run Pharmaceuticals, LLC	70436-213	70436-0213-82
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Slate Run Pharmaceuticals, LLC	70436-216	70436-0216-51
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Slate Run Pharmaceuticals, LLC	70436-217	70436-0217-80
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Slate Run Pharmaceuticals, LLC	70436-216	70436-0216-81
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Slate Run Pharmaceuticals, LLC	70436-217	70436-0217-50

All 17 gadobutrol NDCs

Other NDCs under ANDA 219287

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

FDA NDC Directory listings under ANDA 219287
Product	Strength	Form · route	Labeler	Product NDC
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Zydus Pharmaceuticals USA Inc.	70710-2064
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Zydus Pharmaceuticals USA Inc.	70710-2065
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Viwit Pharmaceutical Co., Ltd.	42337-006
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Viwit Pharmaceutical Co., Ltd.	42337-005
gadobutrol	Gadobutrol 604.72 mg/mL	InjectionIntravenous	Viwit Pharmaceutical Co., Ltd.	42337-007