NDC codes

FDA NDC Directory
Product NDC (as listed)42806-058Labeler and product segments. Claims need a package NDC.
Product NDC at billing width42806-0058Add 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
42806-058-0142806005801100 TABLET in 1 BOTTLE (42806-058-01)Marketed from Feb 21, 2011
42806-058-10428060058101000 TABLET in 1 BOTTLE (42806-058-10)Marketed from Feb 21, 2011

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)
Flavoxate Hydrochloride
Generic name (nonproprietary)
flavoxate hydrochloride
Active ingredients
Flavoxate hydrochloride — 100 mg/1
Dosage form
Tablet
Route
Oral
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 076835
Marketing start
Listing expires
Other FDA classes
Cholinergic Muscarinic Antagonists (Mechanism)
Identifiers
Product ID 42806-058_6aeb8856-3df7-40a7-b03e-d855a58c8fa4SPL ID 6aeb8856-3df7-40a7-b03e-d855a58c8fa4SPL set ID b4260d7e-2ab3-49f6-aa57-bae19a23d82aRxCUI 1095229UNII 9C05J6089WUPC 0342806058015
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

N442806005801 followed by a unit qualifier and the quantity

Package 42806-0058-01. 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 076835

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

FDA NDC Directory listings under ANDA 076835
ProductStrengthForm · routeLabelerProduct NDC
Flavoxate HydrochlorideFlavoxate hydrochloride 100 mg/1TabletOralPuraCap Laboratories LLC dba Blu Pharmaceuticals24658-720

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