NDC codes

FDA NDC Directory
Product NDC (as listed)0904-7027Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00904-7027Add 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
0904-7027-610090470276100904702761100 BLISTER PACK in 1 CARTON (0904-7027-61) / 1 TABLET in 1 BLISTER PACKMarketed from Nov 15, 2017

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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
Major PharmaceuticalsNDC labeler code 0904
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 209823
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 0904-7027_dfc72462-93cb-4e29-bd55-dbd31a4b5b84SPL ID dfc72462-93cb-4e29-bd55-dbd31a4b5b84SPL set ID 7769ad3d-6228-4b2d-8f44-4efe990d3fadRxCUI 863664UNII L9F3D9RENQ
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

N400904702761 followed by a unit qualifier and the quantity

Package 00904-7027-61. 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 & USAGE Oxybutynin chloride tablets, USP are 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 0904-7027

What is NDC 0904-7027?
0904-7027 is the product NDC for Oxybutynin Chloride, Oxybutynin chloride 5 mg/1 tablet, listed with the FDA by Major Pharmaceuticals. 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?
Major Pharmaceuticals, NDC labeler code 0904. 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 209823

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

FDA NDC Directory listings under ANDA 209823
ProductStrengthForm · routeLabelerProduct NDC
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralA-S Medication Solutions50090-6966
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralA-S Medication Solutions50090-6967
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralGolden State Medical Supply, Inc.51407-099
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralNorthwind Health Company, LLC51655-665
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralCardinal Health 107, LLC55154-2632
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralNuCare Pharmaceuticals,Inc.66267-642
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralANI Pharmaceuticals, Inc.70954-005
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralAphena Pharma Solutions - Tennessee, LLC71610-277
Oxybutynin ChlorideOxybutynin chloride 5 mg/1TabletOralVERITYRX, LLC83939-0022

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