What is NDC 0990-7905?

0990-7905 is the product NDC for Potassium Chloride in Dextrose, Dextrose monohydrate 5 g/100mL; Potassium chloride .149 g/100mL injection, solution, listed with the FDA by ICU Medical Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.

What drug is associated with this NDC?

Potassium Chloride in Dextrose (Dextrose monohydrate and potassium chloride injection, solution).

What is the active ingredient?

Dextrose monohydrate, Potassium chloride.

ICU Medical Inc., NDC labeler code 0990. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Potassium Chloride in Dextrose?

2 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Potassium Chloride in Dextrose NDC 0990-7905

NDC codes

FDA NDC Directory

Product NDC (as listed)0990-7905Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00990-7905Add 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
0990-7905-09	00990790509	12 POUCH in 1 CASE (0990-7905-09) / 1 BAG in 1 POUCH / 1000 mL in 1 BAGMarketed from Nov 20, 2020

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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): Potassium Chloride in Dextrose
Generic name (nonproprietary): dextrose monohydrate and potassium chloride injection, solution
Active ingredients: Dextrose monohydrate — 5 g/100mLPotassium chloride — .149 g/100mL
Dosage form: Injection, Solution
Route: Intravenous
Labeler: ICU Medical Inc.NDC labeler code 0990
Product type: Prescription drug
Marketing category: NDA — New Drug ApplicationApplication NDA 018371
Marketing start: Nov 20, 2020
Listing expires: Dec 31, 2027
Other FDA classes: Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)
Identifiers: Product ID 0990-7905_f342a90d-8637-42b9-add5-e6875e700d3bSPL ID f342a90d-8637-42b9-add5-e6875e700d3bSPL set ID 02d694b5-3600-4d55-bd5c-924abaec5315RxCUI 309783UNII LX22YL083G, 660YQ98I10
Pharmacologic class: Osmotic Laxative; Potassium Salt

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

N400990790509 followed by a unit qualifier and the quantity

Package 00990-7905-09. 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 Oct 30, 2025.

Indications (excerpt from the label)

INDICATIONS AND USAGE This solution is indicated in patients requiring parenteral administration of potassium chloride with minimal carbohydrate calories.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0990-7905

What is NDC 0990-7905?: 0990-7905 is the product NDC for Potassium Chloride in Dextrose, Dextrose monohydrate 5 g/100mL; Potassium chloride .149 g/100mL injection, solution, listed with the FDA by ICU Medical Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Potassium Chloride in Dextrose (Dextrose monohydrate and potassium chloride injection, solution).
What is the active ingredient?: Dextrose monohydrate, Potassium chloride.
Who is the labeler?: ICU Medical Inc., NDC labeler code 0990. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Potassium Chloride in Dextrose?: 2 other product NDCs are listed under this name. See all Potassium Chloride in Dextrose 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 Potassium Chloride in Dextrose NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Potassium Chloride In Dextrosedextrose and potassium chloride	Dextrose 5 g/100mL; Potassium chloride .15 g/100mL	SolutionIntravenous	B. Braun Medical Inc.	0264-7625	00264-7625-00
Potassium Chloride in Dextrosepotassium chloride and dextrose monohydrate	Potassium chloride 150 mg/100mL; Dextrose monohydrate 5 g/100mL	Injection, SolutionIntravenous	Baxter Healthcare Company	0338-0683	00338-0683-04