Package 84549-631-25

Brand: atropine sulfate

Generic: atropine sulfate
NDC Package

Package Facts

Identity

Package NDC 84549-631-25
Digits Only 8454963125
Product NDC 84549-631
Description

1 mL in 1 VIAL (84549-631-25)

Marketing

Marketing Status
Marketed Since 2025-09-16
Brand atropine sulfate
Generic atropine sulfate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3eef6300-9c77-82b2-e063-6294a90a5499", "openfda": {"unii": ["03J5ZE7KA5"], "rxcui": ["1666781"], "spl_set_id": ["3eef6300-9c78-82b2-e063-6294a90a5499"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL (84549-631-25)", "package_ndc": "84549-631-25", "marketing_start_date": "20250916"}], "brand_name": "Atropine Sulfate", "product_id": "84549-631_3eef6300-9c77-82b2-e063-6294a90a5499", "dosage_form": "SOLUTION", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "84549-631", "generic_name": "Atropine Sulfate", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atropine Sulfate", "active_ingredients": [{"name": "ATROPINE SULFATE", "strength": ".4 mg/mL"}], "application_number": "ANDA215969", "marketing_category": "ANDA", "marketing_start_date": "20240704", "listing_expiration_date": "20261231"}