NDC codes

FDA NDC Directory
Product NDC (as listed)80830-1692Labeler and product segments. Claims need a package NDC.
Product NDC at billing width80830-1692Add 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
80830-1692-28083016920210 VIAL in 1 CARTON (80830-1692-2) / 50 mL in 1 VIAL (80830-1692-1)Marketed from Oct 23, 2023
80830-1692-58083016920525 VIAL in 1 CARTON (80830-1692-5) / 50 mL in 1 VIAL (80830-1692-1)Marketed from Oct 23, 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)
Potassium Phosphates
Generic name (nonproprietary)
potassium phosphate, monobasic potassium phosphate, dibasic injection,
Active ingredients
Potassium phosphate, Monobasic — 224 mg/mLPotassium phosphate, Dibasic — 236 mg/mL
Dosage form
Solution, Concentrate
Route
Intravenous
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 216344
Marketing start
Listing expires
Other FDA classes
Increased Large Intestinal Motility (Physiologic effect)Increased Large Intestinal Motility (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Inhibition Large Intestine Fluid/Electrolyte Absorption (Physiologic effect)Osmotic Activity (Mechanism)Osmotic Activity (Mechanism)Potassium Compounds (Chemical structure)Potassium Compounds (Chemical structure)
Identifiers
Product ID 80830-1692_d20a884f-9cba-4621-91ee-6e0ba6e361caSPL ID d20a884f-9cba-4621-91ee-6e0ba6e361caSPL set ID 89136c51-a60b-4269-bd05-9489f060a734RxCUI 1928567, 1928569, 1928570UNII 4J9FJ0HL51, CI71S98N1ZUPC 0380830169253
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

N480830169202 followed by a unit qualifier and the quantity

Package 80830-1692-02. 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 .

Indications (excerpt from the label)

Potassium phosphates injection is indicated as a source of phosphorus: in intravenous fluids to correct hypophosphatemia in adults and pediatric patients when oral or enteral replacement is not possible, insufficient or contraindicated. for parenteral nutrition in adults and pediatric patients when oral or enteral nutrition is not possible, insufficient or contraindicated. Potassium phosphates injection is a phosphorus replacement product indicated as a source of phosphorus: in intravenous fluids to correct hypophosphatemia in adults and pediatric patients when oral or enteral replacement is not possible, insufficient or contraindicated. ( 1 ) for parenteral nutrition in adults and pediatric…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under ANDA 216344

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

FDA NDC Directory listings under ANDA 216344
ProductStrengthForm · routeLabelerProduct NDC
Potassium Phosphatespotassium phosphate, monobasic potassium phosphate, dibasic injection,Potassium phosphate, Monobasic 224 mg/mL; Potassium phosphate, Dibasic 236 mg/mLSolution, ConcentrateIntravenousAmneal Pharmaceuticals Private Limited80830-1691
Potassium Phosphatespotassium phosphate, monobasic potassium phosphate, dibasic injection,Potassium phosphate, Monobasic 224 mg/mL; Potassium phosphate, Dibasic 236 mg/mLSolution, ConcentrateIntravenousAmneal Pharmaceuticals Private Limited80830-1693
Potassium Phosphatespotassium phosphate, monobasic potassium phosphate, dibasic injection,Potassium phosphate, Monobasic 224 mg/mL; Potassium phosphate, Dibasic 236 mg/mLSolution, ConcentrateIntravenousAmneal Pharmaceuticals Private Limited80830-1691
Potassium Phosphatespotassium phosphate, monobasic potassium phosphate, dibasic injection,Potassium phosphate, Monobasic 224 mg/mL; Potassium phosphate, Dibasic 236 mg/mLSolution, ConcentrateIntravenousAmneal Pharmaceuticals Private Limited80830-1691

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