liothyronine sodium
Generic: liothyronine sodium
Labeler: northstar rx llcDrug Facts
Product Profile
Brand Name
liothyronine sodium
Generic Name
liothyronine sodium
Labeler
northstar rx llc
Dosage Form
TABLET
Routes
Active Ingredients
liothyronine sodium 5 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
16714-166
Product ID
16714-166_215d81f8-589d-490f-a470-8c50fb7aad65
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA214803
Listing Expiration
2026-12-31
Marketing Start
2021-05-05
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
16714166
Hyphenated Format
16714-166
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
liothyronine sodium (source: ndc)
Generic Name
liothyronine sodium (source: ndc)
Application Number
ANDA214803 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 ug/1
Packaging
- 100 TABLET in 1 BOTTLE (16714-166-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "215d81f8-589d-490f-a470-8c50fb7aad65", "openfda": {"upc": ["0316714166018", "0316714167015"], "unii": ["GCA9VV7D2N"], "rxcui": ["903456", "903697", "903703"], "spl_set_id": ["c97dc9ec-af73-4836-aa0d-c27e66e792a9"], "manufacturer_name": ["Northstar Rx LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET in 1 BOTTLE (16714-166-01)", "package_ndc": "16714-166-01", "marketing_start_date": "20210505"}], "brand_name": "Liothyronine sodium", "product_id": "16714-166_215d81f8-589d-490f-a470-8c50fb7aad65", "dosage_form": "TABLET", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "16714-166", "generic_name": "Liothyronine sodium", "labeler_name": "Northstar Rx LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Liothyronine sodium", "active_ingredients": [{"name": "LIOTHYRONINE SODIUM", "strength": "5 ug/1"}], "application_number": "ANDA214803", "marketing_category": "ANDA", "marketing_start_date": "20210505", "listing_expiration_date": "20261231"}