levothyroxine sodium
Generic: levothyroxine sodium
Labeler: redpharm drugDrug Facts
Product Profile
Brand Name
levothyroxine sodium
Generic Name
levothyroxine sodium
Labeler
redpharm drug
Dosage Form
TABLET
Routes
Active Ingredients
levothyroxine sodium 100 ug/1
Manufacturer
Identifiers & Regulatory
Product NDC
67296-2048
Product ID
67296-2048_2c631fd1-ba23-5863-e063-6394a90a75a8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212399
Listing Expiration
2026-12-31
Marketing Start
2020-12-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
672962048
Hyphenated Format
67296-2048
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
- 100 ug/1
Packaging
- 30 TABLET in 1 BOTTLE (67296-2048-3)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2c631fd1-ba23-5863-e063-6394a90a75a8", "openfda": {"upc": ["0316729447157", "0316729449151", "0316729452151", "0316729454155", "0316729453158", "0316729448154", "0316729451154", "0316729457156", "0316729450157", "0316729456159", "0316729458153", "0316729455152"], "unii": ["9J765S329G"], "rxcui": ["892246"], "spl_set_id": ["fa2aebcd-3cd8-5128-e053-6294a90ac612"], "manufacturer_name": ["Redpharm drug"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (67296-2048-3)", "package_ndc": "67296-2048-3", "marketing_start_date": "20201210"}], "brand_name": "Levothyroxine sodium", "product_id": "67296-2048_2c631fd1-ba23-5863-e063-6394a90a75a8", "dosage_form": "TABLET", "pharm_class": ["Thyroxine [CS]", "l-Thyroxine [EPC]"], "product_ndc": "67296-2048", "generic_name": "Levothyroxine Sodium", "labeler_name": "Redpharm drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Levothyroxine sodium", "active_ingredients": [{"name": "LEVOTHYROXINE SODIUM", "strength": "100 ug/1"}], "application_number": "ANDA212399", "marketing_category": "ANDA", "marketing_start_date": "20201210", "listing_expiration_date": "20261231"}