NDC codes

FDA NDC Directory
Product NDC (as listed)64380-918Labeler and product segments. Claims need a package NDC.
Product NDC at billing width64380-0918Add 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
64380-918-0664380091806100 TABLET in 1 BOTTLE (64380-918-06)Marketed from Feb 8, 2021

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)
Ursodiol
Generic name (nonproprietary)
ursodiol
Active ingredients
Ursodiol — 250 mg/1
Dosage form
Tablet
Route
Oral
Labeler
Strides Pharma Science LimitedNDC labeler code 64380
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 213504
Marketing start
Listing expires
Other FDA classes
Bile Acids and Salts (Chemical structure)
Identifiers
Product ID 64380-918_3e523229-7dbb-4a1d-908e-3ead0f4081cbSPL ID 3e523229-7dbb-4a1d-908e-3ead0f4081cbSPL set ID 9d666bbc-98c4-445f-a5a2-cad1bcccde4eRxCUI 858733, 858751UNII 724L30Y2QRUPC 0364380918066, 0364380919063
Pharmacologic class
Bile Acid

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

N464380091806 followed by a unit qualifier and the quantity

Package 64380-0918-06. 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)

Ursodiol tablets, 250 mg and 500 mg are indicated for the treatment of patients with primary biliary cholangitis (PBC). Ursodiol tablets, 250 mg and 500 mg are bile acids indicated for the treatment of patients with primary biliary cholangitis.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 64380-918

What is NDC 64380-918?
64380-918 is the product NDC for Ursodiol, Ursodiol 250 mg/1 tablet, listed with the FDA by Strides Pharma Science Limited. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ursodiol.
What is the active ingredient?
Ursodiol.
Who is the labeler?
Strides Pharma Science Limited, NDC labeler code 64380. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ursodiol?
41 other product NDCs are listed under this name. See all Ursodiol 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 Ursodiol NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
UrsodiolUrsodiol 300 mg/1CapsuleOralAvPAK50268-86450268-0864-13
UrsodiolUrsodiol 300 mg/1CapsuleOralNorthStar Rx LLC72603-61372603-0613-01
UrsodiolUrsodiol 250 mg/1Tablet, Film coatedOralCardinal Health 107, LLC55154-263355154-2633-00
UrsodiolUrsodiol 500 mg/1Tablet, Film coatedOralAvKARE42291-93142291-0931-01
UrsodiolUrsodiol 300 mg/1CapsuleOralAvKARE42291-92342291-0923-01
UrsodiolUrsodiol 300 mg/1CapsuleOralBryant Ranch Prepack72162-261972162-2619-01
UrsodiolUrsodiol 300 mg/1CapsuleOralPuraCap Laboratories, LLC24658-99924658-0999-10
UrsodiolUrsodiol 300 mg/1CapsuleOralStrides Pharma Science Limited64380-84464380-0844-0464380-0844-0664380-0844-07
UrsodiolUrsodiol 300 mg/1CapsuleOralLaurus Labs Limited42385-94642385-0946-01
UrsodiolUrsodiol 300 mg/1CapsuleOralAvPAK50268-79750268-0797-15

All 42 Ursodiol NDCs

Other NDCs under ANDA 213504

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

FDA NDC Directory listings under ANDA 213504
ProductStrengthForm · routeLabelerProduct NDC
UrsodiolUrsodiol 500 mg/1TabletOralStrides Pharma Science Limited64380-919

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