NDC codes

FDA NDC Directory
Product NDC (as listed)63629-1967Labeler and product segments. Claims need a package NDC.
Product NDC at billing width63629-1967Add 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
63629-1967-163629196701100 TABLET, EXTENDED RELEASE in 1 BOTTLE (63629-1967-1)Marketed from Feb 8, 2022

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 Citrate
Generic name (nonproprietary)
potassium citrate
Active ingredients
Potassium citrate — 15 meq/1
Dosage form
Tablet, Extended release
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212779
Marketing start
Listing expires
Other FDA classes
Acidifying Activity (Mechanism)Calcium Chelating Activity (Mechanism)Decreased Coagulation Factor Activity (Physiologic effect)
Identifiers
Product ID 63629-1967_72a84600-76b3-4803-ad0d-737680420295SPL ID 72a84600-76b3-4803-ad0d-737680420295SPL set ID f2ab3c2e-2a6e-4698-afad-260bdf0d259eRxCUI 898490UNII EE90ONI6FF
Pharmacologic class
Anti-coagulant; Calculi Dissolution Agent

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

N463629196701 followed by a unit qualifier and the quantity

Package 63629-1967-01. 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

Label details couldn’t be retrieved right now. Open the label on DailyMed.

Other NDCs under ANDA 212779

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

FDA NDC Directory listings under ANDA 212779
ProductStrengthForm · routeLabelerProduct NDC
Potassium CitratePotassium citrate 10 meq/1Tablet, Extended releaseOralBryant Ranch Prepack72162-1758
Potassium CitratePotassium citrate 15 meq/1Tablet, Extended releaseOralBryant Ranch Prepack72162-1759
Potassium CitratePotassium citrate 10 meq/1Tablet, Extended releaseOralREMEDYREPACK INC.70518-3160
Potassium CitratePotassium citrate 10 meq/1Tablet, Extended releaseOralANI Pharmaceuticals, Inc.62559-291
Potassium CitratePotassium citrate 15 meq/1Tablet, Extended releaseOralANI Pharmaceuticals, Inc.62559-292
Potassium CitratePotassium citrate 10 meq/1Tablet, Extended releaseOralBryant Ranch Prepack71335-1967
Potassium CitratePotassium citrate 10 meq/1Tablet, Extended releaseOralBryant Ranch Prepack63629-1966

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