Package 70069-829-01
Brand: nitrofurantoin
Generic: nitrofurantoinPackage Facts
Identity
Package NDC
70069-829-01
Digits Only
7006982901
Product NDC
70069-829
Description
1 BOTTLE, GLASS in 1 CARTON (70069-829-01) / 230 mL in 1 BOTTLE, GLASS
Marketing
Marketing Status
Brand
nitrofurantoin
Generic
nitrofurantoin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "40efa147-f323-4d77-9a88-227434ff84c3", "openfda": {"nui": ["N0000175494", "M0014892"], "unii": ["927AH8112L"], "rxcui": ["311989"], "spl_set_id": ["dd99ba40-edff-47c3-9ee4-7e5b7774e5b5"], "pharm_class_cs": ["Nitrofurans [CS]"], "pharm_class_epc": ["Nitrofuran Antibacterial [EPC]"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (70069-829-01) / 230 mL in 1 BOTTLE, GLASS", "package_ndc": "70069-829-01", "marketing_start_date": "20250226"}], "brand_name": "Nitrofurantoin", "product_id": "70069-829_40efa147-f323-4d77-9a88-227434ff84c3", "dosage_form": "FOR SUSPENSION", "pharm_class": ["Nitrofuran Antibacterial [EPC]", "Nitrofurans [CS]"], "product_ndc": "70069-829", "generic_name": "Nitrofurantoin", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nitrofurantoin", "active_ingredients": [{"name": "NITROFURANTOIN", "strength": "25 mg/5mL"}], "application_number": "ANDA208909", "marketing_category": "ANDA", "marketing_start_date": "20250226", "listing_expiration_date": "20271231"}