NDC codes

FDA NDC Directory
Product NDC (as listed)62207-727Labeler and product segments. Claims need a package NDC.
Product NDC at billing width62207-0727Add 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
62207-727-086220707270862207072708800 TABLET in 1 BOTTLE (62207-727-08)Marketed from Jan 30, 2021
62207-727-436220707274362207072743100 TABLET in 1 BOTTLE (62207-727-43)Marketed from Jan 30, 2021
62207-727-476220707274762207072747500 TABLET in 1 BOTTLE (62207-727-47)Marketed from Jan 30, 2021
62207-727-4962207072749622070727491000 TABLET in 1 BOTTLE (62207-727-49)Marketed from Jun 25, 2021
62207-727-57622070727576220707275790 TABLET in 1 BOTTLE (62207-727-57)Marketed from Jan 30, 2021

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 Extended-release
Generic name (nonproprietary)
potassium chloride extended-release
Active ingredients
Potassium chloride — 1500 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Granules India LtdNDC labeler code 62207
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 214452
Marketing start
Listing expires
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 62207-727_5d3e685a-6b4c-1ac8-e063-6394a90a9ad9SPL ID 5d3e685a-6b4c-1ac8-e063-6394a90a9ad9
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 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

N462207072708 followed by a unit qualifier and the quantity

Package 62207-0727-08. 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 62207-727

What is NDC 62207-727?
62207-727 is the product NDC for Potassium Chloride Extended-release, Potassium chloride 1500 mg/1 tablet, listed with the FDA by Granules India Ltd. It has 5 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Potassium Chloride Extended-release.
What is the active ingredient?
Potassium chloride.
Who is the labeler?
Granules India Ltd, NDC labeler code 62207. 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 Extended-release?
45 other product NDCs are listed under this name. See all Potassium Chloride Extended-release 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 Extended-release NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralMajor Pharmaceuticals0904-754700904-7547-61
Potassium Chloride Extended Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-452070518-4520-00
Potassium Chloride Extended-releasePotassium chloride 1500 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-438370518-4383-0070518-4383-0170518-4383-02
Potassium Chloride Extended Releasepotassium chloridePotassium chloride 600 mg/1Tablet, Extended releaseOralRising Pharma Holdings, Inc.16571-84216571-0842-0116571-0842-1016571-0842-50
Potassium Chloride Extended Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralRising Pharma Holdings, Inc.16571-84316571-0843-0116571-0843-1016571-0843-50
Potassium Chloride Extended-releasePotassium chloride 750 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-409570518-4095-0270518-4095-03
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralUpsher-Smith Laboratories, LLC24979-23124979-0231-0124979-0231-0224979-0231-03
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 1500 mg/1Tablet, Extended releaseOralUpsher-Smith Laboratories, LLC24979-23224979-0232-0124979-0232-02
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-663950090-6639-0050090-6639-0150090-6639-02+1 more
Potassium Chloride Extended-Releasepotassium chloridePotassium chloride 750 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-664050090-6640-00

All 46 Potassium Chloride Extended-release NDCs

Other NDCs under ANDA 214452

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

FDA NDC Directory listings under ANDA 214452
ProductStrengthForm · routeLabelerProduct NDC
Potassium Chloride ERPotassium chloride 1500 mg/1Tablet, Extended releaseOralDirect_Rx72189-629
Potassium Chloride ERPotassium chloride 750 mg/1Tablet, Extended releaseOralDirect_Rx72189-648
Potassium Chloride Extended-ReleasePotassium chloride 750 mg/1Tablet, Extended releaseOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8399
Potassium Chloride Extended-ReleasePotassium chloride 1500 mg/1Tablet, Extended releaseOralNCS HealthCare of KY, LLC dba Vangard Labs0615-8400
Potassium Chloride Extended-releasePotassium chloride 1500 mg/1Tablet, Extended releaseOralAtlantic Biologicals Corp.17856-1135
Potassium Chloride Extended-releasePotassium chloride 1500 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-7192
Potassium Chloride Extended-releasePotassium chloride 1500 mg/1Tablet, Extended releaseOralA-S Medication Solutions50090-7193
Potassium Chloride Extended-releasePotassium chloride 750 mg/1TabletOralGranules India Ltd62207-726
Potassium Chloride Extended-releasePotassium chloride 1500 mg/1Tablet, Extended releaseOralRedpharm Drug67296-2160
Potassium Chloride Extended-releasePotassium chloride 750 mg/1TabletOralBluepoint Laboratories68001-566
Potassium Chloride Extended-releasePotassium chloride 1500 mg/1TabletOralBluepoint Laboratories68001-567
Potassium Chloride Extended-releasePotassium chloride 1500 mg/1Tablet, Extended releaseOralPreferred Pharmaceuticals Inc.68788-8196
Potassium Chloride Extended-releasePotassium chloride 1500 mg/1Tablet, Extended releaseOralGranules Pharmaceuticals Inc.70010-135
Potassium Chloride Extended-releasePotassium chloride 750 mg/1Tablet, Extended releaseOralGranules Pharmaceuticals Inc.70010-136
Potassium Chloride Extended-releasePotassium chloride 750 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-4095
Potassium Chloride Extended-releasePotassium chloride 1500 mg/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-4383
Potassium Chloride Extended-releasePotassium chloride 1500 mg/1Tablet, Extended releaseOralProficient Rx LP71205-824
Potassium Chloride Extended-releasePotassium chloride 1500 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-1896
Potassium Chloride Extended-releasePotassium chloride 750 mg/1Tablet, Extended releaseOralBryant Ranch Prepack71335-2503
Potassium Chloride Extended-releasePotassium chloride 750 mg/1Tablet, Extended releaseOralProficient Rx LP82804-109

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