What is NDC 51754-0103?

51754-0103 is the product NDC for Cupric Chloride, Cupric chloride .4 mg/mL injection, solution, listed with the FDA by Exela Pharma Sciences, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.

Exela Pharma Sciences, LLC, NDC labeler code 51754. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Cupric Chloride?

5 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Cupric Chloride NDC 51754-0103 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)51754-0103Labeler and product segments. Claims need a package NDC.

Product NDC at billing width51754-0103Add 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
51754-0103-3	51754010303	10 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-3) / 10 mL in 1 VIAL, SINGLE-DOSEMarketed from Feb 1, 2023
51754-0103-4	51754010304	25 VIAL, SINGLE-DOSE in 1 CARTON (51754-0103-4) / 10 mL in 1 VIAL, SINGLE-DOSEMarketed from Feb 1, 2023

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): Cupric Chloride
Generic name (nonproprietary): cupric chloride
Active ingredients: Cupric chloride — .4 mg/mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: Exela Pharma Sciences, LLCNDC labeler code 51754
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 212071
Marketing start: Feb 1, 2023
Listing expires: Dec 31, 2026
Identifiers: Product ID 51754-0103_18dc9e1c-b9db-4160-96f7-8c4391bcf8c9SPL ID 18dc9e1c-b9db-4160-96f7-8c4391bcf8c9SPL set ID daaa6f3a-148e-4f1c-bd44-bb2242145b88RxCUI 204536UNII S2QG84156O

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

N451754010303 followed by a unit qualifier and the quantity

Package 51754-0103-03. 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 May 16, 2019.

Indications (excerpt from the label)

INDICATIONS AND USAGE Cupric Chloride Injection, USP 0.4 mg/mL is indicated for use as a supplement to intravenous solutions given for total parenteral nutrition (TPN). Administration helps to maintain copper serum levels and to prevent depletion of endogenous stores and subsequent deficiency symptoms.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 51754-0103

What is NDC 51754-0103?: 51754-0103 is the product NDC for Cupric Chloride, Cupric chloride .4 mg/mL injection, solution, listed with the FDA by Exela Pharma Sciences, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Cupric Chloride.
What is the active ingredient?: Cupric chloride.
Who is the labeler?: Exela Pharma Sciences, LLC, NDC labeler code 51754. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Cupric Chloride?: 5 other product NDCs are listed under this name. See all Cupric 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 Cupric Chloride NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Cupric Chloride	Cupric chloride .4 mg/mL	Injection, SolutionIntravenous	Renova Pharmaceuticals LLC	84897-013	84897-0013-25
Cupric Chloride	Cupric chloride .4 mg/mL	Injection, SolutionIntravenous	Amneal Pharmaceuticals Private Limited	80830-2301	80830-2301-05
Cupric Chloride	Cupric chloride .4 mg/mL	Injection, SolutionIntravenous	Northstar Rx LLC	72603-351	72603-0351-25
Cupric Chloride	Cupric chloride .4 mg/mL	Injection, SolutionIntravenous	Archis Pharma LLC	72819-234	72819-0234-99
Cupric Chloride	Cupric chloride .4 mg/mL	InjectionIntravenous	Somerset Therapeutics, LLC	70069-506	70069-0506-25