What is NDC 0480-8710?

0480-8710 is the product NDC for Levothyroxine sodium, Levothyroxine sodium 137 ug/1 tablet, listed with the FDA by Teva Pharmaceuticals, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.

Teva Pharmaceuticals, Inc., NDC labeler code 0480. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Levothyroxine sodium?

517 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Levothyroxine sodium NDC 0480-8710

NDC codes

FDA NDC Directory

Product NDC (as listed)0480-8710Labeler and product segments. Claims need a package NDC.

Product NDC at billing width00480-8710Add 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
0480-8710-10	0048087101000480871010	1000 TABLET in 1 BOTTLE (0480-8710-10)Marketed from Sep 21, 2022
0480-8710-98	0048087109800480871098	90 TABLET in 1 BOTTLE (0480-8710-98)Marketed from Sep 21, 2022

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): Levothyroxine sodium
Generic name (nonproprietary): levothyroxine sodium
Active ingredients: Levothyroxine sodium — 137 ug/1
Dosage form: Tablet
Route: Oral
Labeler: Teva Pharmaceuticals, Inc.NDC labeler code 0480
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 207588
Marketing start: Sep 21, 2022
Marketing end: Nov 30, 2026
Other FDA classes: Thyroxine (Chemical structure)
Identifiers: Product ID 0480-8710_8f65417f-488f-4e4a-894c-56f99ed57d25SPL ID 8f65417f-488f-4e4a-894c-56f99ed57d25SPL set ID 60cadfd7-82b5-4207-97e1-1dd0655efb27RxCUI 892246, 892251, 892255, 966220, 966221, 966222, 966224, 966225, 966248, 966249, 966253, 966270UNII 9J765S329GUPC 0304808704987, 0304808725982, 0304808690983, 0304808718984, 0304808715983, 0304808682988, 0304808693984
Pharmacologic class: l-Thyroxine

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

N400480871010 followed by a unit qualifier and the quantity

Package 00480-8710-10. 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 1, 2024. This label includes a boxed warning.

Indications (excerpt from the label)

Hypothyroidism Levothyroxine sodium tablets are indicated in adult and pediatric patients, including neonates, as a replacement therapy in primary (thyroidal), secondary (pituitary), and tertiary (hypothalamic) congenital or acquired hypothyroidism. Pituitary Thyrotropin (Thyroid-Stimulating Hormone, TSH) Suppression Levothyroxine sodium tablets are indicated in adult and pediatric patients, including neonates, as an adjunct to surgery and radioiodine therapy in the management of thyrotropin-dependent well-differentiated thyroid cancer. Limitations of Use Levothyroxine sodium tablets are not indicated for suppression of benign thyroid nodules and nontoxic diffuse goiter in iodine-sufficient …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 0480-8710

What is NDC 0480-8710?: 0480-8710 is the product NDC for Levothyroxine sodium, Levothyroxine sodium 137 ug/1 tablet, listed with the FDA by Teva Pharmaceuticals, Inc.. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Levothyroxine sodium.
What is the active ingredient?: Levothyroxine sodium.
Who is the labeler?: Teva Pharmaceuticals, Inc., NDC labeler code 0480. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Levothyroxine sodium?: 517 other product NDCs are listed under this name. See all Levothyroxine sodium 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 Levothyroxine sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Levothyroxine Sodium	Levothyroxine sodium .05 mg/1	TabletOral	Coupler LLC	67046-0819	67046-0819-03
Levothyroxine Sodium	Levothyroxine sodium .137 mg/1	TabletOral	Coupler LLC	67046-0972	67046-0972-03
Levothyroxine Sodium	Levothyroxine sodium .2 mg/1	TabletOral	Coupler LLC	67046-0387	67046-0387-03
Levothyroxine Sodium	Levothyroxine sodium .125 mg/1	TabletOral	Coupler LLC	67046-0951	67046-0951-03
Levothyroxine Sodium	Levothyroxine sodium 100 ug/1	TabletOral	Coupler LLC	67046-1679	67046-1679-03
Levothyroxine Sodium	Levothyroxine sodium .175 mg/1	TabletOral	Coupler LLC	67046-0517	67046-0517-03
Levothyroxine Sodium	Levothyroxine sodium .15 mg/1	TabletOral	Coupler LLC	67046-0515	67046-0515-03
Levothyroxine Sodium	Levothyroxine sodium .1 mg/1	TabletOral	Coupler LLC	67046-0569	67046-0569-03
Levothyroxine Sodium	Levothyroxine sodium .075 mg/1	TabletOral	Coupler LLC	67046-0801	67046-0801-03
Levothyroxine Sodium	Levothyroxine sodium .112 mg/1	TabletOral	Coupler LLC	67046-0290	67046-0290-03

All 518 Levothyroxine sodium NDCs

Other NDCs under ANDA 207588

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

FDA NDC Directory listings under ANDA 207588
Product	Strength	Form · route	Labeler	Product NDC
Levothyroxine sodium	Levothyroxine sodium 75 ug/1	TabletOral	Teva Pharmaceuticals, Inc.	0480-8690
Levothyroxine sodium	Levothyroxine sodium 88 ug/1	TabletOral	Teva Pharmaceuticals, Inc.	0480-8693
Levothyroxine sodium	Levothyroxine sodium 112 ug/1	TabletOral	Teva Pharmaceuticals, Inc.	0480-8704
Levothyroxine sodium	Levothyroxine sodium 175 ug/1	TabletOral	Teva Pharmaceuticals, Inc.	0480-8718
Levothyroxine sodium	Levothyroxine sodium 200 ug/1	TabletOral	Teva Pharmaceuticals, Inc.	0480-8722
Levothyroxine sodium	Levothyroxine sodium 112 ug/1	TabletOral	A-S Medication Solutions	50090-7526
Levothyroxine sodium	Levothyroxine sodium 112 ug/1	TabletOral	A-S Medication Solutions	50090-7527
Levothyroxine sodium	Levothyroxine sodium 200 ug/1	TabletOral	A-S Medication Solutions	50090-7937
Levothyroxine sodium	Levothyroxine sodium 88 ug/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8792
Levothyroxine sodium	Levothyroxine sodium 200 ug/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-8902
Levothyroxine sodium	Levothyroxine sodium 88 ug/1	TabletOral	Bryant Ranch Prepack	71335-2538
Levothyroxine sodium	Levothyroxine sodium 137 ug/1	TabletOral	Bryant Ranch Prepack	71335-2562
Levothyroxine sodium	Levothyroxine sodium 50 ug/1	TabletOral	Proficient Rx LP	82804-149