liothyronine sodium
Generic: liothyronine sodium
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
liothyronine sodium
Generic Name
liothyronine sodium
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
liothyronine sodium 25 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-884
Product ID
43063-884_415c6ae0-9636-3fb9-e063-6394a90accdc
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA200295
Listing Expiration
2026-12-31
Marketing Start
2012-12-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063884
Hyphenated Format
43063-884
Supplemental Identifiers
RxCUI
UPC
UNII
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
ANDA200295 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 ug/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (43063-884-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "415c6ae0-9636-3fb9-e063-6394a90accdc", "openfda": {"upc": ["0343063884300"], "unii": ["GCA9VV7D2N"], "rxcui": ["903697"], "spl_set_id": ["76fa4eb6-fefa-4e97-9543-f81e465743e6"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (43063-884-30)", "package_ndc": "43063-884-30", "marketing_start_date": "20180816"}], "brand_name": "Liothyronine Sodium", "product_id": "43063-884_415c6ae0-9636-3fb9-e063-6394a90accdc", "dosage_form": "TABLET", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "43063-884", "generic_name": "Liothyronine Sodium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Liothyronine Sodium", "active_ingredients": [{"name": "LIOTHYRONINE SODIUM", "strength": "25 ug/1"}], "application_number": "ANDA200295", "marketing_category": "ANDA", "marketing_start_date": "20121203", "listing_expiration_date": "20261231"}