Package 51662-1341-1

Brand: aminophylline

Generic: aminophylline
NDC Package

Package Facts

Identity

Package NDC 51662-1341-1
Digits Only 5166213411
Product NDC 51662-1341
Description

20 mL in 1 VIAL, SINGLE-DOSE (51662-1341-1)

Marketing

Marketing Status
Marketed Since 2019-02-10
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": "1057db94-30a8-224a-e063-6394a90a020d", "openfda": {"unii": ["C229N9DX94"], "rxcui": ["1724666"], "spl_set_id": ["819207a2-0c37-b275-e053-2a91aa0afb36"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, SINGLE-DOSE (51662-1341-1)", "package_ndc": "51662-1341-1", "marketing_start_date": "20190210"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1341-3)  / 1 mL in 1 POUCH (51662-1341-2)", "package_ndc": "51662-1341-3", "marketing_start_date": "20201027"}], "brand_name": "AMINOPHYLLINE", "product_id": "51662-1341_1057db94-30a8-224a-e063-6394a90a020d", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Methylxanthine [EPC]", "Xanthines [CS]"], "product_ndc": "51662-1341", "generic_name": "AMINOPHYLLINE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "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": "20190210", "listing_expiration_date": "20261231"}