What is NDC 43598-925?

43598-925 is the product NDC for Sugammadex, Sugammadex sodium 500 mg/5mL injection, solution, listed with the FDA by Dr. Reddy's Laboratories Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

Dr. Reddy's Laboratories Inc., NDC labeler code 43598. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Sugammadex?

35 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Sugammadex NDC 43598-925 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)43598-925Labeler and product segments. Claims need a package NDC.

Product NDC at billing width43598-0925Add 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
43598-925-37	4359809253743598092537	10 VIAL, SINGLE-DOSE in 1 CARTON (43598-925-37) / 5 mL in 1 VIAL, SINGLE-DOSE (43598-925-11)Marketed from Jul 28, 2026

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): Sugammadex
Generic name (nonproprietary): sugammadex
Active ingredients: Sugammadex sodium — 500 mg/5mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: Dr. Reddy's Laboratories Inc.NDC labeler code 43598
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 214236
Marketing start: Jul 28, 2026
Listing expires: Dec 31, 2027
Other FDA classes: gamma-Cyclodextrins (Chemical structure)
Identifiers: Product ID 43598-925_449d5f1e-0c01-473e-689c-556eb007aeb3SPL ID 449d5f1e-0c01-473e-689c-556eb007aeb3SPL set ID 4f90c37e-3505-0968-38fd-fc7e4dd66e82RxCUI 1726992, 1727000UNII ERJ6X2MXV7

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

N443598092537 followed by a unit qualifier and the quantity

Package 43598-0925-37. 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 Feb 18, 2026.

Indications (excerpt from the label)

Sugammadex injection is indicated for the reversal of neuromuscular blockade induced by rocuronium bromide and vecuronium bromide in adult and pediatric patients aged 2 years and older undergoing surgery. Additional pediatric use information is approved for Merck Sharp & Dohme LLC’s BRIDION ® (sugammadex) injection. However, due to Merck Sharp & Dohme LLC’s marketing exclusivity rights, this drug product is not labeled with that information. Sugammadex injection is indicated for the reversal of neuromuscular blockade induced by rocuronium bromide and vecuronium bromide in adult and pediatric patients aged 2 years and older undergoing surgery. (1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43598-925

What is NDC 43598-925?: 43598-925 is the product NDC for Sugammadex, Sugammadex sodium 500 mg/5mL injection, solution, listed with the FDA by Dr. Reddy's Laboratories Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Sugammadex.
What is the active ingredient?: Sugammadex sodium.
Who is the labeler?: Dr. Reddy's Laboratories Inc., NDC labeler code 43598. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Sugammadex?: 35 other product NDCs are listed under this name. See all Sugammadex 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 Sugammadex NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
sugammadex	Sugammadex sodium 200 mg/2mL	Injection, SolutionIntravenous	Accord Healthcare Inc.	16729-726	16729-0726-03
sugammadex	Sugammadex sodium 500 mg/5mL	Injection, SolutionIntravenous	Accord Healthcare Inc.	16729-727	16729-0727-03
sugammadex	Sugammadex sodium 200 mg/2mL	Injection, SolutionIntravenous	Fosun Pharma USA Inc.	72266-268	72266-0268-10
sugammadex	Sugammadex sodium 500 mg/5mL	Injection, SolutionIntravenous	Fosun Pharma USA Inc.	72266-269	72266-0269-10
Sugammadex	Sugammadex sodium 200 mg/2mL	InjectionIntravenous	B. Braun Medical Inc.	0264-8200	00264-8200-10
Sugammadex	Sugammadex sodium 100 mg/mL	InjectionIntravenous	Hikma Pharmaceuticals USA Inc.	0641-6270	00641-6270-10
Sugammadex	Sugammadex sodium 200 mg/2mL	Injection, SolutionIntravenous	Sandoz Inc	0781-3468	00781-3468-95
Sugammadex	Sugammadex sodium 500 mg/5mL	Injection, SolutionIntravenous	Sandoz Inc	0781-3469	00781-3469-95
Sugammadex	Sugammadex sodium 200 mg/2mL	Injection, SolutionIntravenous	Dr. Reddy's Laboratories Inc.	43598-924	43598-0924-26
sugammadexsugammadex sodium	Sugammadex sodium 100 mg/mL	Injection, SolutionIntravenous	Solupharm Pharmazeutische Erzeugnisse GmbH	55579-892	55579-0892-10

All 36 Sugammadex NDCs

Other NDCs under ANDA 214236

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

FDA NDC Directory listings under ANDA 214236
Product	Strength	Form · route	Labeler	Product NDC
Sugammadex	Sugammadex sodium 200 mg/2mL	Injection, SolutionIntravenous	Dr. Reddy's Laboratories Inc.	43598-924