Package 70069-716-01

Brand: atropine sulfate

Generic: atropine sulfate monohydrate
NDC Package

Package Facts

Identity

Package NDC 70069-716-01
Digits Only 7006971601
Product NDC 70069-716
Description

1 BOTTLE in 1 CARTON (70069-716-01) / 5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-05-24
Brand atropine sulfate
Generic atropine sulfate monohydrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["OPHTHALMIC"], "spl_id": "07ece291-b401-4c28-9c81-6b686aa36e07", "openfda": {"upc": ["0370069716014"], "unii": ["03J5ZE7KA5"], "rxcui": ["1190655"], "spl_set_id": ["bfdb85b2-86d0-4f32-a8fa-272af48a191c"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70069-716-01)  / 5 mL in 1 BOTTLE", "package_ndc": "70069-716-01", "marketing_start_date": "20240524"}], "brand_name": "Atropine Sulfate", "product_id": "70069-716_07ece291-b401-4c28-9c81-6b686aa36e07", "dosage_form": "SOLUTION/ DROPS", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "70069-716", "generic_name": "Atropine Sulfate Monohydrate", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atropine Sulfate", "active_ingredients": [{"name": "ATROPINE SULFATE", "strength": "10 mg/mL"}], "application_number": "ANDA217791", "marketing_category": "ANDA", "marketing_start_date": "20240524", "listing_expiration_date": "20261231"}