What is NDC 49884-413?

49884-413 is the product NDC for Ursodiol, Ursodiol 500 mg/1 tablet, film coated, listed with the FDA by Par Health USA, LLC. It has 1 package NDC, shown above in 10- and 11-digit form.

Par Health USA, LLC, NDC labeler code 49884. 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.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Ursodiol NDC 49884-413 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)49884-413Labeler and product segments. Claims need a package NDC.

Product NDC at billing width49884-0413Add 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 NDC	11-digit (billing)	Package	Copy
49884-413-01	49884041301	100 TABLET, FILM COATED in 1 BOTTLE (49884-413-01)Marketed from Aug 1, 2013

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 — 500 mg/1
Dosage form: Tablet, Film coated
Route: Oral
Labeler: Par Health USA, LLCNDC labeler code 49884
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 202540
Marketing start: Aug 1, 2013
Listing expires: Dec 31, 2027
Other FDA classes: Bile Acids and Salts (Chemical structure)
Identifiers: Product ID 49884-413_a215d03f-22c2-438f-b383-508aa5d7ef51SPL ID a215d03f-22c2-438f-b383-508aa5d7ef51SPL set ID 1a3a8942-94d4-4292-bf74-0a67d92acb90RxCUI 858733, 858751UNII 724L30Y2QRUPC 0349884412012
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

N449884041301 followed by a unit qualifier and the quantity

Package 49884-0413-01. 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

Current FDA label (SPL), effective Jun 12, 2026.

Indications (excerpt from the label)

Ursodiol tablets are indicated for the treatment of patients with primary biliary cholangitis (PBC). Ursodiol tablets are bile acids indicated for the treatment of patients with primary biliary cholangitis. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 49884-413

What is NDC 49884-413?: 49884-413 is the product NDC for Ursodiol, Ursodiol 500 mg/1 tablet, film coated, listed with the FDA by Par Health USA, LLC. 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?: Par Health USA, LLC, NDC labeler code 49884. 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
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Ursodiol	Ursodiol 300 mg/1	CapsuleOral	AvPAK	50268-864	50268-0864-13
Ursodiol	Ursodiol 300 mg/1	CapsuleOral	NorthStar Rx LLC	72603-613	72603-0613-01
Ursodiol	Ursodiol 250 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-2633	55154-2633-00
Ursodiol	Ursodiol 500 mg/1	Tablet, Film coatedOral	AvKARE	42291-931	42291-0931-01
Ursodiol	Ursodiol 300 mg/1	CapsuleOral	AvKARE	42291-923	42291-0923-01
Ursodiol	Ursodiol 300 mg/1	CapsuleOral	Bryant Ranch Prepack	72162-2619	72162-2619-01
Ursodiol	Ursodiol 300 mg/1	CapsuleOral	PuraCap Laboratories, LLC	24658-999	24658-0999-10
Ursodiol	Ursodiol 300 mg/1	CapsuleOral	Strides Pharma Science Limited	64380-844	64380-0844-0464380-0844-0664380-0844-07
Ursodiol	Ursodiol 300 mg/1	CapsuleOral	Laurus Labs Limited	42385-946	42385-0946-01
Ursodiol	Ursodiol 300 mg/1	CapsuleOral	AvPAK	50268-797	50268-0797-15

All 42 Ursodiol NDCs

Other NDCs under ANDA 202540

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

FDA NDC Directory listings under ANDA 202540
Product	Strength	Form · route	Labeler	Product NDC
Ursodiol	Ursodiol 250 mg/1	Tablet, Film coatedOral	Major Pharmaceuticals	0904-6890
Ursodiol	Ursodiol 500 mg/1	Tablet, Film coatedOral	AvKARE	42291-931
Ursodiol	Ursodiol 250 mg/1	Tablet, Film coatedOral	Par Health USA, LLC	49884-412
Ursodiol	Ursodiol 250 mg/1	Tablet, Film coatedOral	Cardinal Health 107, LLC	55154-2633
Ursodiol	Ursodiol 250 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-2286
Ursodiol	Ursodiol 500 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	63629-2287
Ursodiol	Ursodiol 250 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-1500
Ursodiol	Ursodiol 500 mg/1	Tablet, Film coatedOral	Bryant Ranch Prepack	72162-1501