What is NDC 71205-150?

71205-150 is the product NDC for Liothyronine Sodium, Liothyronine sodium 5 ug/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.

Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.

What other NDCs exist for Liothyronine Sodium?

44 other product NDCs are listed under this name.

Is there a related HCPCS / J-code?

Not in Med-Code's curated HCPCS directory.

Liothyronine Sodium NDC 71205-150 | National Drug Code

NDC codes

FDA NDC Directory

Product NDC (as listed)71205-150Labeler and product segments. Claims need a package NDC.

Product NDC at billing width71205-0150Add 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
71205-150-30	7120501503071205015030	30 TABLET in 1 BOTTLE (71205-150-30)Marketed from Nov 1, 2018
71205-150-60	7120501506071205015060	60 TABLET in 1 BOTTLE (71205-150-60)Marketed from Nov 1, 2018
71205-150-90	7120501509071205015090	90 TABLET in 1 BOTTLE (71205-150-90)Marketed from Nov 1, 2018

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): Liothyronine Sodium
Generic name (nonproprietary): liothyronine sodium
Active ingredients: Liothyronine sodium — 5 ug/1
Dosage form: Tablet
Route: Oral
Labeler: Proficient Rx LPNDC labeler code 71205
Product type: Prescription drug
Marketing category: ANDA — Abbreviated New Drug Application (generic)Application ANDA 200295
Marketing start: Dec 3, 2012
Listing expires: Dec 31, 2027
Other FDA classes: Triiodothyronine (Chemical structure)
Identifiers: Product ID 71205-150_7c4088ea-921d-440c-ae1c-c473fc381e50SPL ID 7c4088ea-921d-440c-ae1c-c473fc381e50SPL set ID f882d34f-6b9f-4d9d-8a3e-3054ba91c506RxCUI 903456UNII GCA9VV7D2NUPC 0371205150303
Pharmacologic class: l-Triiodothyronine

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

N471205015030 followed by a unit qualifier and the quantity

Package 71205-0150-30. 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 Jul 1, 2023. This label includes a boxed warning.

Indications (excerpt from the label)

INDICATIONS AND USAGE Thyroid hormone drugs are indicated: 1. As replacement or supplemental therapy in patients with hypothyroidism of any etiology, except transient hypothyroidism during the recovery phase of subacute thyroiditis. This category includes cretinism, myxedema and ordinary hypothyroidism in patients of any age (pediatric patients, adults, the elderly), or state (including pregnancy); primary hypothyroidism resulting from functional deficiency, primary atrophy, partial or total absence of thyroid gland, or the effects of surgery, radiation, or drugs, with or without the presence of goiter; and secondary (pituitary) or tertiary (hypothalamic) hypothyroidism (see WARNINGS ). 2. A…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 71205-150

What is NDC 71205-150?: 71205-150 is the product NDC for Liothyronine Sodium, Liothyronine sodium 5 ug/1 tablet, listed with the FDA by Proficient Rx LP. It has 3 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?: Liothyronine Sodium.
What is the active ingredient?: Liothyronine sodium.
Who is the labeler?: Proficient Rx LP, NDC labeler code 71205. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Liothyronine Sodium?: 44 other product NDCs are listed under this name. See all Liothyronine 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 Liothyronine Sodium NDCs
Product	Strength	Form · route	Labeler	Product NDC	Package NDCs (11-digit)
Liothyronine Sodium	Liothyronine sodium 25 ug/1	TabletOral	Dr. Reddy's Labratories Inc.	75907-001	75907-0001-01
Liothyronine Sodium	Liothyronine sodium 50 ug/1	TabletOral	Dr. Reddy's Labratories Inc.	75907-004	75907-0004-01
Liothyronine Sodium	Liothyronine sodium 5 ug/1	TabletOral	Dr. Reddy's Labratories Inc.	75907-039	75907-0039-01
Liothyronine sodium	Liothyronine sodium 5 ug/1	TabletOral	Biocon Pharma Inc.	70377-114	70377-0114-1170377-0114-1270377-0114-13
Liothyronine sodium	Liothyronine sodium 25 ug/1	TabletOral	Biocon Pharma Inc.	70377-115	70377-0115-1170377-0115-1270377-0115-13
Liothyronine sodium	Liothyronine sodium 50 ug/1	TabletOral	Biocon Pharma Inc.	70377-116	70377-0116-1170377-0116-1270377-0116-13
Liothyronine sodium	Liothyronine sodium 5 ug/1	TabletOral	Northstar Rx LLC	16714-166	16714-0166-01
Liothyronine sodium	Liothyronine sodium 25 ug/1	TabletOral	Northstar Rx LLC	16714-167	16714-0167-01
Liothyronine sodium	Liothyronine sodium 50 ug/1	TabletOral	Northstar Rx LLC	16714-168	16714-0168-01
Liothyronine Sodium	Liothyronine sodium 25 ug/1	TabletOral	Teva Pharmaceuticals USA, Inc.	0093-2178	00093-2178-01

All 45 Liothyronine Sodium NDCs

Other NDCs under ANDA 200295

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

FDA NDC Directory listings under ANDA 200295
Product	Strength	Form · route	Labeler	Product NDC
Liomnyliothyronine sodium	Liothyronine sodium 5 ug/1	TabletOral	SIGMAPHARM LABORATORIES, LLC	42794-131
Liomnyliothyronine sodium	Liothyronine sodium 25 ug/1	TabletOral	SIGMAPHARM LABORATORIES, LLC	42794-132
Liomnyliothyronine sodium	Liothyronine sodium 50 ug/1	TabletOral	SIGMAPHARM LABORATORIES, LLC	42794-133
Liothyronine Sodium	Liothyronine sodium 5 ug/1	TabletOral	SIGMAPHARM LABORATORIES, LLC	42794-018
Liothyronine Sodium	Liothyronine sodium 25 ug/1	TabletOral	SIGMAPHARM LABORATORIES, LLC	42794-019
Liothyronine Sodium	Liothyronine sodium 50 ug/1	TabletOral	SIGMAPHARM LABORATORIES, LLC	42794-020
Liothyronine Sodium	Liothyronine sodium 25 ug/1	TabletOral	PD-Rx Pharmaceuticals, Inc.	43063-884
Liothyronine Sodium	Liothyronine sodium 5 ug/1	TabletOral	A-S Medication Solutions	50090-3131
Liothyronine Sodium	Liothyronine sodium 5 ug/1	TabletOral	NuCare Pharmaceuticals,Inc.	68071-3571
Liothyronine Sodium	Liothyronine sodium 5 ug/1	TabletOral	Preferred Pharmaceuticals Inc.	68788-7269
Liothyronine Sodium	Liothyronine sodium 25 ug/1	TabletOral	Bryant Ranch Prepack	71335-0166
Liothyronine Sodium	Liothyronine sodium 5 ug/1	TabletOral	Bryant Ranch Prepack	71335-0341
Liothyronine Sodium	Liothyronine sodium 50 ug/1	TabletOral	Bryant Ranch Prepack	71335-9632
Liothyronine Sodium	Liothyronine sodium 5 ug/1	TabletOral	ASCLEMED USA INC.	87063-080
Liothyronine Sodium	Liothyronine sodium 25 ug/1	TabletOral	ASCLEMED USA INC.	87063-081
Liothyronine Sodium	Liothyronine sodium 50 ug/1	TabletOral	ASCLEMED USA INC.	87063-082