NDC codes

FDA NDC Directory
Product NDC (as listed)43063-931Labeler and product segments. Claims need a package NDC.
Product NDC at billing width43063-0931Add 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
43063-931-30430630931304306309313030 TABLET in 1 BOTTLE, PLASTIC (43063-931-30)Marketed from Jan 9, 2019

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)
Oxybutynin Chloride
Generic name (nonproprietary)
oxybutynin chloride
Active ingredients
Oxybutynin chloride — 5 mg/1
Dosage form
Tablet
Route
Oral
Labeler
PD-Rx Pharmaceuticals, Inc.NDC labeler code 43063
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209335
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 43063-931_302c054b-7dcb-1396-e063-6394a90ac66eSPL ID 302c054b-7dcb-1396-e063-6394a90ac66eSPL set ID 9c8ced4b-94de-4df8-bea3-b42b8846b769RxCUI 863664UNII L9F3D9RENQUPC 0343063931301
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

N443063093130 followed by a unit qualifier and the quantity

Package 43063-0931-30. 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)

INDICATIONS AND USAGE Oxybutynin chloride is indicated for the relief of symptoms of bladder instability associated with voiding in patients with uninhibited neurogenic or reflex neurogenic bladder (i.e., urgency, frequency, urinary leakage, urge incontinence, dysuria).

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 43063-931

What is NDC 43063-931?
43063-931 is the product NDC for Oxybutynin Chloride, Oxybutynin chloride 5 mg/1 tablet, listed with the FDA by PD-Rx Pharmaceuticals, Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Oxybutynin Chloride.
What is the active ingredient?
Oxybutynin chloride.
Who is the labeler?
PD-Rx Pharmaceuticals, Inc., NDC labeler code 43063. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Oxybutynin Chloride?
79 other product NDCs are listed under this name. See all Oxybutynin Chloride 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 Oxybutynin Chloride NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Oxybutynin ChlorideOxybutynin chloride 2.5 mg/1TabletOralTruPharma LLC52817-26152817-0261-10
Oxybutynin ChlorideOxybutynin chloride 2.5 mg/1TabletOralRISING PHARMA HOLDINGS, INC.64980-73464980-0734-01
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralCoupler LLC67046-138167046-1381-03
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralHeritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.23155-91323155-0913-0123155-0913-0523155-0913-10
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralRISING PHARMA HOLDINGS, INC.64980-67964980-0679-0164980-0679-1064980-0679-50
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralA-S Medication Solutions50090-807850090-8078-0050090-8078-0150090-8078-03
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralAmerican Health Packaging60687-89960687-0899-01
Oxybutynin ChlorideOxybutynin chloride 2.5 mg/1TabletOralStrides Pharma Science Limited64380-19064380-0190-01
Oxybutynin ChlorideOxybutynin chloride 15 mg/1Tablet, Extended releaseOralCoupler LLC67046-160067046-1600-03
Oxybutynin ChlorideOxybutynin chloride 5 mg/1Tablet, Extended releaseOralCoupler LLC67046-159967046-1599-03

All 80 Oxybutynin Chloride NDCs

Other NDCs under ANDA 209335

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

FDA NDC Directory listings under ANDA 209335
ProductStrengthForm · routeLabelerProduct NDC
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralKVK-Tech, Inc.10702-201
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralPD-Rx Pharmaceuticals, Inc.43063-851
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralA-S Medication Solutions50090-4622
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralPreferred Pharmaceuticals Inc.68788-8141
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralREMEDYREPACK INC.70518-2640
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralBryant Ranch Prepack71335-1494
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralNorthwind Health Company, LLC82868-047

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