Package 84549-922-01

Brand: aminophylline

Generic: aminophylline
NDC Package

Package Facts

Identity

Package NDC 84549-922-01
Digits Only 8454992201
Product NDC 84549-922
Description

20 mL in 1 VIAL, SINGLE-DOSE (84549-922-01)

Marketing

Marketing Status
Marketed Since 2025-09-17
Brand aminophylline
Generic aminophylline
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "463df5df-3086-2160-e063-6294a90ac75f", "openfda": {"unii": ["C229N9DX94"], "rxcui": ["1724666"], "spl_set_id": ["3f000254-a9f1-c8c7-e063-6394a90aa33f"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, SINGLE-DOSE (84549-922-01)", "package_ndc": "84549-922-01", "marketing_start_date": "20250917"}], "brand_name": "Aminophylline", "product_id": "84549-922_463df5df-3086-2160-e063-6294a90ac75f", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "84549-922", "generic_name": "Aminophylline", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Aminophylline", "active_ingredients": [{"name": "AMINOPHYLLINE DIHYDRATE", "strength": "25 mg/mL"}], "application_number": "ANDA087242", "marketing_category": "ANDA", "marketing_start_date": "20050228", "listing_expiration_date": "20261231"}