NDC codes

FDA NDC Directory
Product NDC (as listed)43066-129Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43066-0129Add 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
43066-129-0543066012905430660129055 CARTON in 1 CARTON (43066-129-05) / 1 SYRINGE, PLASTIC in 1 CARTON (43066-129-01) / 10 mL in 1 SYRINGE, PLASTICMarketed from Sep 24, 2024

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)
Succinylcholine Chloride
Generic name (nonproprietary)
succinylcholine chloride
Active ingredients
Succinylcholine chloride dihydrate — 20 mg/mL
Dosage form
Injection, Solution
Route
Intramuscular, Intravenous
Labeler
Baxter Healthcare CorporationNDC labeler code 43066
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 218878
Marketing start
Listing expires
Other FDA classes
Neuromuscular Depolarizing Blockade (Physiologic effect)
Identifiers
Product ID 43066-129_3b9ee5c1-e92b-4ebe-98d2-d3d6ffe3dd1cSPL ID 3b9ee5c1-e92b-4ebe-98d2-d3d6ffe3dd1cSPL set ID 30f58922-3c74-4813-ace0-fcd2024acd09RxCUI 2598128, 2694114UNII 8L0S1G435E
Pharmacologic class
Depolarizing Neuromuscular Blocker

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

N443066012905 followed by a unit qualifier and the quantity

Package 43066-0129-05. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

About NDC 43066-129

What is NDC 43066-129?
43066-129 is the product NDC for Succinylcholine Chloride, Succinylcholine chloride dihydrate 20 mg/mL injection, solution, listed with the FDA by Baxter Healthcare Corporation. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Succinylcholine Chloride.
What is the active ingredient?
Succinylcholine chloride dihydrate.
Who is the labeler?
Baxter Healthcare Corporation, NDC labeler code 43066. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Succinylcholine Chloride?
31 other product NDCs are listed under this name. See all Succinylcholine Chloride 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 Succinylcholine Chloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Succinylcholine ChlorideSuccinylcholine chloride 20 mg/mLInjection, SolutionIntramuscular, IntravenousREMEDYREPACK INC.70518-440970518-4409-00
Succinylcholine ChlorideSuccinylcholine chloride dihydrate 20 mg/mLInjection, SolutionIntramuscular, IntravenousFresenius Kabi USA LLC65219-27465219-0274-05
Succinylcholine ChlorideSuccinylcholine chloride dihydrate 20 mg/mLInjection, SolutionIntramuscular, IntravenousFresenius Kabi USA LLC65219-27665219-0276-10
Succinylcholine ChlorideSuccinylcholine chloride 20 mg/mLInjection, SolutionIntramuscular, IntravenousSTERISCIENCE SPECIALTIES PRIVATE LIMITED82449-23282449-0232-02
Succinylcholine ChlorideSuccinylcholine chloride dihydrate 20 mg/mLInjection, SolutionIntramuscular, IntravenousBaxter Healthcare Corporation43066-12743066-0127-05
Succinylcholine ChlorideSuccinylcholine chloride 20 mg/mLInjection, SolutionIntramuscular, IntravenousDevatis, Inc.73043-02173043-0021-01
Succinylcholine ChlorideSuccinylcholine chloride 20 mg/mLInjection, SolutionIntramuscular, IntravenousEugia US LLC55150-31555150-0315-25
Succinylcholine ChlorideSuccinylcholine chloride 20 mg/mLInjection, SolutionIntramuscular, IntravenousSomerset Therapeutics, LLC70069-78370069-0783-1070069-0783-25
Succinylcholine ChlorideSuccinylcholine chloride 20 mg/mLInjection, SolutionIntramuscular, IntravenousLifestar Pharma LLC70756-61370756-0613-1070756-0613-25
Succinylcholine ChlorideSuccinylcholine chloride 20 mg/mLInjection, SolutionIntramuscular, IntravenousHenry Schein, Inc.0404-998300404-9983-20

All 32 Succinylcholine Chloride NDCs

Other NDCs under ANDA 218878

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

FDA NDC Directory listings under ANDA 218878
ProductStrengthForm · routeLabelerProduct NDC
Succinylcholine ChlorideSuccinylcholine chloride dihydrate 20 mg/mLInjection, SolutionIntramuscular, IntravenousBaxter Healthcare Corporation43066-127

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