levothyroxine sodium
Generic: levothyroxine sodium
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
levothyroxine sodium
Generic Name
levothyroxine sodium
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
levothyroxine sodium 50 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-272
Product ID
72789-272_4bad91ed-0e19-2d1e-e063-6394a90a669f
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212399
Listing Expiration
2027-12-31
Marketing Start
2020-11-25
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789272
Hyphenated Format
72789-272
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
levothyroxine sodium (source: ndc)
Generic Name
levothyroxine sodium (source: ndc)
Application Number
ANDA212399 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 ug/1
Packaging
- 30 TABLET in 1 BOTTLE, PLASTIC (72789-272-30)
- 90 TABLET in 1 BOTTLE, PLASTIC (72789-272-90)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4bad91ed-0e19-2d1e-e063-6394a90a669f", "openfda": {"upc": ["0372789272900"], "unii": ["9J765S329G"], "rxcui": ["966221"], "spl_set_id": ["70a9bb5c-2259-405e-8d89-cc1db8c70743"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-272-30)", "package_ndc": "72789-272-30", "marketing_start_date": "20220916"}, {"sample": false, "description": "90 TABLET in 1 BOTTLE, PLASTIC (72789-272-90)", "package_ndc": "72789-272-90", "marketing_start_date": "20220923"}], "brand_name": "Levothyroxine sodium", "product_id": "72789-272_4bad91ed-0e19-2d1e-e063-6394a90a669f", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "72789-272", "generic_name": "Levothyroxine Sodium", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "50 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20201125", "listing_expiration_date": "20271231"}