NDC codes

FDA NDC Directory
Product NDC (as listed)16729-726Labeler and product segments. Claims need a package NDC.
Product NDC at billing width16729-0726Add 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
16729-726-03167290726031672907260310 VIAL, SINGLE-DOSE in 1 CARTON (16729-726-03) / 2 mL in 1 VIAL, SINGLE-DOSEMarketed from Aug 4, 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 — 200 mg/2mL
Dosage form
Injection, Solution
Route
Intravenous
Labeler
Accord Healthcare Inc.NDC labeler code 16729
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214306
Marketing start
Listing expires
Other FDA classes
gamma-Cyclodextrins (Chemical structure)
Identifiers
Product ID 16729-726_584eff57-3033-e86e-e063-6394a90aa30fSPL ID 584eff57-3033-e86e-e063-6394a90aa30fSPL set ID 57bf9b96-0550-b8e4-e063-6294a90a317bRxCUI 1726992, 1727000UNII ERJ6X2MXV7UPC 0316729726030

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

N416729072603 followed by a unit qualifier and the quantity

Package 16729-0726-03. 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)

Sugammadex 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 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 16729-726

What is NDC 16729-726?
16729-726 is the product NDC for sugammadex, Sugammadex sodium 200 mg/2mL injection, solution, listed with the FDA by Accord Healthcare 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?
Accord Healthcare Inc., NDC labeler code 16729. 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
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
sugammadexSugammadex sodium 500 mg/5mLInjection, SolutionIntravenousAccord Healthcare Inc.16729-72716729-0727-03
sugammadexSugammadex sodium 200 mg/2mLInjection, SolutionIntravenousFosun Pharma USA Inc.72266-26872266-0268-10
sugammadexSugammadex sodium 500 mg/5mLInjection, SolutionIntravenousFosun Pharma USA Inc.72266-26972266-0269-10
SugammadexSugammadex sodium 200 mg/2mLInjectionIntravenousB. Braun Medical Inc.0264-820000264-8200-10
SugammadexSugammadex sodium 100 mg/mLInjectionIntravenousHikma Pharmaceuticals USA Inc.0641-627000641-6270-10
SugammadexSugammadex sodium 200 mg/2mLInjection, SolutionIntravenousSandoz Inc0781-346800781-3468-95
SugammadexSugammadex sodium 500 mg/5mLInjection, SolutionIntravenousSandoz Inc0781-346900781-3469-95
SugammadexSugammadex sodium 200 mg/2mLInjection, SolutionIntravenousDr. Reddy's Laboratories Inc.43598-92443598-0924-26
SugammadexSugammadex sodium 500 mg/5mLInjection, SolutionIntravenousDr. Reddy's Laboratories Inc.43598-92543598-0925-37
sugammadexsugammadex sodiumSugammadex sodium 100 mg/mLInjection, SolutionIntravenousSolupharm Pharmazeutische Erzeugnisse GmbH55579-89255579-0892-10

All 36 sugammadex NDCs

Other NDCs under ANDA 214306

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

FDA NDC Directory listings under ANDA 214306
ProductStrengthForm · routeLabelerProduct NDC
sugammadexSugammadex sodium 500 mg/5mLInjection, SolutionIntravenousAccord Healthcare Inc.16729-727

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