NDC codes

FDA NDC Directory
Product NDC (as listed)50090-8078Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-8078Add 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
50090-8078-05009080780030 TABLET in 1 BOTTLE (50090-8078-0)Marketed from Sep 16, 2026
50090-8078-150090807801100 TABLET in 1 BOTTLE (50090-8078-1)Marketed from Sep 16, 2026
50090-8078-35009080780390 TABLET in 1 BOTTLE (50090-8078-3)Marketed from Sep 16, 2026

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)
Oxybutynin Chloride
Generic name (nonproprietary)
oxybutynin chloride
Active ingredients
Oxybutynin chloride — 5 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209025
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 50090-8078_0fe86fc9-7a70-4911-9567-74da2b585e75SPL ID 0fe86fc9-7a70-4911-9567-74da2b585e75
Pharmacologic class
Cholinergic Muscarinic Antagonist

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

N450090807800 followed by a unit qualifier and the quantity

Package 50090-8078-00. 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.

Other NDCs under ANDA 209025

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

FDA NDC Directory listings under ANDA 209025
ProductStrengthForm · routeLabelerProduct NDC
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralA-S Medication Solutions50090-6638
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralRISING PHARMA HOLDINGS, INC.64980-431
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-490
Oxybutynin ChlorideOxybutynin chloride 2.5 mg/1TabletOralRISING PHARMA HOLDINGS, INC.64980-531
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralBryant Ranch Prepack71335-1014
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralRISING PHARMA HOLDINGS, INC.64980-679
Oxybutynin ChlorideOxybutynin chloride 2.5 mg/1TabletOralRISING PHARMA HOLDINGS, INC.64980-734
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralA-S Medication Solutions50090-7766
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.72789-417

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Oxybutynin Chloride NDC 50090-8078 | Med-Code