Package 71335-9632-1
Brand: liothyronine sodium
Generic: liothyronine sodiumPackage Facts
Identity
Package NDC
71335-9632-1
Digits Only
7133596321
Product NDC
71335-9632
Description
30 TABLET in 1 BOTTLE (71335-9632-1)
Marketing
Marketing Status
Brand
liothyronine sodium
Generic
liothyronine sodium
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "7e8ca2e4-1c1e-4565-87a1-cd99437d1dac", "openfda": {"unii": ["GCA9VV7D2N"], "rxcui": ["903703"], "spl_set_id": ["20cbf84d-80f2-4b94-ad47-6aaa362fb4d0"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-9632-1)", "package_ndc": "71335-9632-1", "marketing_start_date": "20230131"}], "brand_name": "Liothyronine Sodium", "product_id": "71335-9632_7e8ca2e4-1c1e-4565-87a1-cd99437d1dac", "dosage_form": "TABLET", "pharm_class": ["Triiodothyronine [CS]", "l-Triiodothyronine [EPC]"], "product_ndc": "71335-9632", "generic_name": "Liothyronine Sodium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Liothyronine Sodium", "active_ingredients": [{"name": "LIOTHYRONINE SODIUM", "strength": "50 ug/1"}], "application_number": "ANDA200295", "marketing_category": "ANDA", "marketing_start_date": "20121203", "listing_expiration_date": "20261231"}