What is NDC 84897-013?

84897-013 is the product NDC for Cupric Chloride, Cupric chloride .4 mg/mL injection, solution, listed with the FDA by Renova Pharmaceuticals LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Renova Pharmaceuticals LLC, NDC labeler code 84897. 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 84897-013 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)84897-013Labeler and product segments. Claims need a package NDC.

Product NDC at billing width84897-0013Add 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
84897-013-25	84897001325	25 VIAL, SINGLE-DOSE in 1 PACKAGE (84897-013-25) / 10 mL in 1 VIAL, SINGLE-DOSE (84897-013-01)Marketed from May 7, 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): Cupric Chloride
Generic name (nonproprietary): cupric chloride
Active ingredients: Cupric chloride — .4 mg/mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: Renova Pharmaceuticals LLCNDC labeler code 84897
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 217626
Marketing start: May 7, 2026
Listing expires: Dec 31, 2027
Identifiers: Product ID 84897-013_7d9f7399-2dfe-4c5a-9946-f011d8a8c6feSPL ID 7d9f7399-2dfe-4c5a-9946-f011d8a8c6feSPL set ID 86bb8a4d-6896-4901-9390-c9a194b6f0cbRxCUI 204536UNII S2QG84156OUPC 0384897013252

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

N484897001325 followed by a unit qualifier and the quantity

Package 84897-0013-25. 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 8, 2026.

Indications (excerpt from the label)

INDICATIONS AND USAGE Cupric chloride injection, USP is indicated for use as a supplement to intravenous solutions given for 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 84897-013

What is NDC 84897-013?: 84897-013 is the product NDC for Cupric Chloride, Cupric chloride .4 mg/mL injection, solution, listed with the FDA by Renova Pharmaceuticals LLC. It has 1 package NDC, 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?: Renova Pharmaceuticals LLC, NDC labeler code 84897. 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	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
Cupric Chloride	Cupric chloride .4 mg/mL	Injection, SolutionIntravenous	Exela Pharma Sciences, LLC	51754-0103	51754-0103-0351754-0103-04

Other NDCs under ANDA 217626

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

FDA NDC Directory listings under ANDA 217626
Product	Strength	Form · route	Labeler	Product NDC
Cupric Chloride	Cupric chloride .4 mg/mL	Injection, SolutionIntravenous	Northstar Rx LLC	72603-351
Cupric Chloride	Cupric chloride .4 mg/mL	Injection, SolutionIntravenous	Archis Pharma LLC	72819-234
Cupric Chloride	Cupric chloride .4 mg/mL	Injection, SolutionIntravenous	Archis Pharma LLC	72819-234