NDC codes

FDA NDC Directory
Product NDC (as listed)70010-071Labeler and product segments. Claims need a package NDC.
Product NDC at billing width70010-0071Add 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
70010-071-4170010007141700100071411.58 g in 1 POUCH (70010-071-41)Marketed from Sep 1, 2023
70010-071-42700100071427001000714230 POUCH in 1 CARTON (70010-071-42) / 1.58 g in 1 POUCHMarketed from Sep 1, 2023
70010-071-437001000714370010007143100 POUCH in 1 CARTON (70010-071-43) / 1.58 g in 1 POUCHMarketed from Sep 1, 2023

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)
Potassium Chloride for Oral Solution
Generic name (nonproprietary)
potassium chloride
Active ingredients
Potassium chloride — 1.5 g/1.58g
Dosage form
For solution
Route
Oral
Labeler
Granules Pharmaceuticals Inc.NDC labeler code 70010
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213467
Marketing start
Listing expires
Identifiers
Product ID 70010-071_5d4eb7da-0961-8928-e063-6394a90ae26aSPL ID 5d4eb7da-0961-8928-e063-6394a90ae26a

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 HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N470010007141 followed by a unit qualifier and the quantity

Package 70010-0071-41. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 70010-071

What is NDC 70010-071?
70010-071 is the product NDC for Potassium Chloride for Oral Solution, Potassium chloride 1.5 g/1.58g for solution, listed with the FDA by Granules Pharmaceuticals Inc.. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Potassium Chloride for Oral Solution (Potassium Chloride).
What is the active ingredient?
Potassium chloride.
Who is the labeler?
Granules Pharmaceuticals Inc., NDC labeler code 70010. 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 for Oral Solution?
6 other product NDCs are listed under this name. See all Potassium Chloride for Oral Solution 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 for Oral Solution NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Potassium Chloride for Oral SolutionPotassium chloride 1.5 g/1.58gPowder, For solutionOralMarlex Pharmaceuticals, Inc.10135-80710135-0807-1310135-0807-15
Potassium Chloride for Oral SolutionPotassium chloride 1.5 g/1.58gSolutionOralMarlex Pharmaceuticals Inc10135-81910135-0819-08
Potassium Chloride for Oral SolutionPotassium chloride 3 g/4.75gSolutionOralMarlex Pharmaceuticals Inc10135-82010135-0820-08
Potassium Chloride for Oral Solutionpotassium chloridePotassium chloride 1.5 g/1.58gFor solutionOralSomerset Therapeutics, LLC70069-82370069-0823-0170069-0823-1070069-0823-30
Potassium Chloride for Oral SolutionPotassium chloride 1.5 g/1.58gPowder, For solutionOralAjenat Pharmaceuticals LLC82983-40382983-0403-1082983-0403-30
Potassium Chloride for Oral SolutionPotassium chloride 1.5 g/1.58gPowder, For solutionOralBPI Labs LLC54288-12554288-0125-1054288-0125-30

Other NDCs under ANDA 213467

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

FDA NDC Directory listings under ANDA 213467
ProductStrengthForm · routeLabelerProduct NDC
Potassium Chloride for Oral Solutionpotassium chloridePotassium chloride 1.5 g/1.58gFor solutionOralSomerset Therapeutics, LLC70069-823

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