Levothyroxine sodium

Product NDC: 71335-1861
11-digit product format: 713351861
Labeler code: 71335
Product ID: 71335-1861_f0dd7f74-bec4-4e66-81ff-202d7890df26
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Levothyroxine Sodium
Dosage form: TABLET
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA212399
Marketing category: ANDA
Marketing start: 2020-11-25
Substance: LEVOTHYROXINE SODIUM
Active strength: 137 ug/1
Pharmacologic classes: Thyroxine [CS], l-Thyroxine [EPC]
NDC exclude flag: No
Listing certified through: 2027-12-31
Current FDA listing: Yes

Additional Listing Data

Finished product: Yes
Brand name base: Levothyroxine sodium
Listing expiration: 2027-12-31

Related Records

DailyMed label linked from SPL set ID

Active Ingredients

Ingredient	Strength
LEVOTHYROXINE SODIUM	137 ug/1

Harmonized Identifiers

Field	Values
Unii	9J765S329G
Rxcui	966270

Related Records

Related UNII Ingredients

UNII	Preferred term	Registry number	Matched term
9J765S329G	LEVOTHYROXINE SODIUM	6106-07-6	LEVOTHYROXINE SODIUM

Packages

Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
71335-1861-1	71335186101	30 TABLET in 1 BOTTLE (71335-1861-1)	30 tablet	2023-02-21	0000-00-00	No	No	Current
71335-1861-2	71335186102	100 TABLET in 1 BOTTLE (71335-1861-2)	100 tablet	2024-12-11	0000-00-00	No	No	Current
71335-1861-3	71335186103	90 TABLET in 1 BOTTLE (71335-1861-3)	90 tablet	2021-05-10	0000-00-00	No	No	Current
71335-1861-4	71335186104	28 TABLET in 1 BOTTLE (71335-1861-4)	28 tablet	2024-12-11	0000-00-00	No	No	Current
71335-1861-5	71335186105	60 TABLET in 1 BOTTLE (71335-1861-5)	60 tablet	2024-12-11	0000-00-00	No	No	Current

Related DailyMed Labels

Title	Manufacturer	Effective date	Type	Version
Levothyroxine sodium	Bryant Ranch Prepack	2026-05-15	HUMAN PRESCRIPTION DRUG LABEL	105