liothyronine sodium

Generic: liothyronine sodium

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name liothyronine sodium
Generic Name liothyronine sodium
Labeler pd-rx pharmaceuticals, inc.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

liothyronine sodium 25 ug/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

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
triiodothyronine [cs] l-triiodothyronine [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43063884
Hyphenated Format 43063-884

Supplemental Identifiers

RxCUI
903697
UPC
0343063884300
UNII
GCA9VV7D2N

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 25 ug/1
source: ndc
Packaging
  • 30 TABLET in 1 BOTTLE, PLASTIC (43063-884-30)
source: ndc

Packages (1)

Ingredients (1)

liothyronine sodium (25 ug/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"}