What is NDC 70518-4409?

70518-4409 is the product NDC for Succinylcholine Chloride, Succinylcholine chloride 20 mg/mL injection, solution, listed with the FDA by REMEDYREPACK INC.. It has 1 package NDC, shown above in 10- and 11-digit form.

REMEDYREPACK INC., NDC labeler code 70518. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Succinylcholine Chloride NDC 70518-4409

NDC codes

FDA NDC Directory

Product NDC (as listed)70518-4409Labeler and product segments. Claims need a package NDC.

Product NDC at billing width70518-4409Add 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
70518-4409-0	7051844090070518440900	10 VIAL in 1 CARTON (70518-4409-0) / 10 mL in 1 VIAL (70518-4409-1)Marketed from Jul 29, 2025

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): Succinylcholine Chloride
Generic name (nonproprietary): succinylcholine chloride
Active ingredients: Succinylcholine chloride — 20 mg/mL
Dosage form: Injection, Solution
Route: Intramuscular, Intravenous
Labeler: REMEDYREPACK INC.NDC labeler code 70518
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 211589
Marketing start: Jul 29, 2025
Listing expires: Dec 31, 2027
Other FDA classes: Neuromuscular Depolarizing Blockade (Physiologic effect)
Identifiers: Product ID 70518-4409_5b22cc2e-1eb3-45ed-e063-6394a90ad257SPL ID 5b22cc2e-1eb3-45ed-e063-6394a90ad257SPL set ID efe5a242-5ba0-4b14-844c-206a79850d81RxCUI 1594589UNII I9L0DDD30I
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

N470518440900 followed by a unit qualifier and the quantity

Package 70518-4409-00. 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 Sep 10, 2026. This label includes a boxed warning.

Indications (excerpt from the label)

Succinylcholine chloride injection is indicated in adults and pediatric patients: as an adjunct to general anesthesia to facilitate tracheal intubation to provide skeletal muscle relaxation during surgery or mechanical ventilation. Succinylcholine chloride injection is a depolarizing neuromuscular blocker indicated in adults and pediatric patients: as an adjunct to general anesthesia (1) to facilitate tracheal intubation (1) to provide skeletal muscle relaxation during surgery or mechanical ventilation. (1)

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 70518-4409

What is NDC 70518-4409?: 70518-4409 is the product NDC for Succinylcholine Chloride, Succinylcholine chloride 20 mg/mL injection, solution, listed with the FDA by REMEDYREPACK INC.. 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.
Who is the labeler?: REMEDYREPACK INC., NDC labeler code 70518. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Succinylcholine Chloride	Succinylcholine chloride dihydrate 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	Fresenius Kabi USA LLC	65219-274	65219-0274-05
Succinylcholine Chloride	Succinylcholine chloride dihydrate 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	Fresenius Kabi USA LLC	65219-276	65219-0276-10
Succinylcholine Chloride	Succinylcholine chloride 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	STERISCIENCE SPECIALTIES PRIVATE LIMITED	82449-232	82449-0232-02
Succinylcholine Chloride	Succinylcholine chloride dihydrate 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	Baxter Healthcare Corporation	43066-127	43066-0127-05
Succinylcholine Chloride	Succinylcholine chloride dihydrate 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	Baxter Healthcare Corporation	43066-129	43066-0129-05
Succinylcholine Chloride	Succinylcholine chloride 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	Devatis, Inc.	73043-021	73043-0021-01
Succinylcholine Chloride	Succinylcholine chloride 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	Eugia US LLC	55150-315	55150-0315-25
Succinylcholine Chloride	Succinylcholine chloride 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	Somerset Therapeutics, LLC	70069-783	70069-0783-1070069-0783-25
Succinylcholine Chloride	Succinylcholine chloride 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	Lifestar Pharma LLC	70756-613	70756-0613-1070756-0613-25
Succinylcholine Chloride	Succinylcholine chloride 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	Henry Schein, Inc.	0404-9983	00404-9983-20

All 32 Succinylcholine Chloride NDCs

Other NDCs under ANDA 211589

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

FDA NDC Directory listings under ANDA 211589
Product	Strength	Form · route	Labeler	Product NDC
Succinylcholine Chloride	Succinylcholine chloride 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	Somerset Therapeutics, LLC	70069-301
Succinylcholine Chloride	Succinylcholine chloride 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	Somerset Therapeutics, LLC	70069-783
Succinylcholine Chloride	Succinylcholine chloride 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	Medical Purchasing Solutions, LLC	71872-7221
Succinylcholine Chloride	Succinylcholine chloride 20 mg/mL	Injection, SolutionIntramuscular, Intravenous	ProPharma Distribution	84549-301