Package 68462-722-05

Brand: theophylline

Generic: theophylline
NDC Package

Package Facts

Identity

Package NDC 68462-722-05
Digits Only 6846272205
Product NDC 68462-722
Description

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-722-05)

Marketing

Marketing Status
Marketed Since 2021-06-03
Brand theophylline
Generic theophylline
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "588a56f6-ac5a-415e-99ac-fdb836e0202f", "openfda": {"nui": ["N0000175790", "M0023046"], "upc": ["0368462721018", "0368462722015"], "unii": ["0I55128JYK"], "rxcui": ["314241", "317769"], "spl_set_id": ["48330a8e-be08-4d38-b8b1-d30fbd5a35de"], "pharm_class_cs": ["Xanthines [CS]"], "pharm_class_epc": ["Methylxanthine [EPC]"], "manufacturer_name": ["Glenmark Pharmaceuticals Inc., USA"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-722-01)", "package_ndc": "68462-722-01", "marketing_start_date": "20210603"}, {"sample": false, "description": "500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-722-05)", "package_ndc": "68462-722-05", "marketing_start_date": "20210603"}, {"sample": false, "description": "30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68462-722-30)", "package_ndc": "68462-722-30", "marketing_start_date": "20210603"}], "brand_name": "Theophylline", "product_id": "68462-722_588a56f6-ac5a-415e-99ac-fdb836e0202f", "dosage_form": "TABLET, EXTENDED RELEASE", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "68462-722", "generic_name": "Theophylline", "labeler_name": "Glenmark Pharmaceuticals Inc., USA", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Theophylline", "active_ingredients": [{"name": "THEOPHYLLINE ANHYDROUS", "strength": "450 mg/1"}], "application_number": "ANDA212184", "marketing_category": "ANDA", "marketing_start_date": "20210603", "listing_expiration_date": "20271231"}