Package 0078-0729-10

Brand: betoptic s

Generic: betaxolol hydrochloride
NDC Package

Package Facts

Identity

Package NDC 0078-0729-10
Digits Only 0078072910
Product NDC 0078-0729
Product ID 0078-0729_c0cc485e-81d4-4204-a894-caa615bea90b
Description

1 BOTTLE in 1 CARTON (0078-0729-10) / 10 mL in 1 BOTTLE

Marketing

Marketing Status
Discontinued 2026-11-30
Brand betoptic s
Generic betaxolol hydrochloride
Sample Package No

Linked Drug Pages (1)

Betoptic S ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["OPHTHALMIC"], "spl_id": "c0cc485e-81d4-4204-a894-caa615bea90b", "openfda": {"unii": ["6X97D2XT0O"], "rxcui": ["213729", "308719"], "spl_set_id": ["905ba189-456c-4aa4-8231-39a971374ad8"], "manufacturer_name": ["Novartis Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (0078-0729-10)  / 10 mL in 1 BOTTLE", "package_ndc": "0078-0729-10", "marketing_end_date": "20261130", "marketing_start_date": "20220803"}, {"sample": false, "description": "1 BOTTLE in 1 CARTON (0078-0729-15)  / 15 mL in 1 BOTTLE", "package_ndc": "0078-0729-15", "marketing_end_date": "20261130", "marketing_start_date": "20220803"}], "brand_name": "Betoptic S", "product_id": "0078-0729_c0cc485e-81d4-4204-a894-caa615bea90b", "dosage_form": "SUSPENSION/ DROPS", "pharm_class": ["Adrenergic beta-Antagonists [MoA]", "beta-Adrenergic Blocker [EPC]"], "product_ndc": "0078-0729", "generic_name": "betaxolol hydrochloride", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Betoptic S", "active_ingredients": [{"name": "BETAXOLOL HYDROCHLORIDE", "strength": "2.8 mg/mL"}], "application_number": "NDA019845", "marketing_category": "NDA", "marketing_end_date": "20261130", "marketing_start_date": "19960115"}