nitrofurantoin
Generic: nitrofurantoin
Labeler: amneal pharmaceuticals ny llcDrug Facts
Product Profile
Brand Name
nitrofurantoin
Generic Name
nitrofurantoin
Labeler
amneal pharmaceuticals ny llc
Dosage Form
SUSPENSION
Routes
Active Ingredients
nitrofurantoin 25 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
69238-2512
Product ID
69238-2512_87af7ed1-6ae7-4eaf-ab35-d46d07549450
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA201679
Listing Expiration
2026-12-31
Marketing Start
2021-05-31
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
692382512
Hyphenated Format
69238-2512
Supplemental Identifiers
RxCUI
UNII
NUI
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
nitrofurantoin (source: ndc)
Generic Name
nitrofurantoin (source: ndc)
Application Number
ANDA201679 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 25 mg/5mL
Packaging
- 1 BOTTLE, GLASS in 1 CARTON (69238-2512-9) / 230 mL in 1 BOTTLE, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "87af7ed1-6ae7-4eaf-ab35-d46d07549450", "openfda": {"nui": ["N0000175494", "M0014892"], "unii": ["927AH8112L"], "rxcui": ["311989"], "spl_set_id": ["80129dba-5939-4292-bfd0-8d53ba165941"], "pharm_class_cs": ["Nitrofurans [CS]"], "pharm_class_epc": ["Nitrofuran Antibacterial [EPC]"], "manufacturer_name": ["Amneal Pharmaceuticals NY LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE, GLASS in 1 CARTON (69238-2512-9) / 230 mL in 1 BOTTLE, GLASS", "package_ndc": "69238-2512-9", "marketing_start_date": "20210531"}], "brand_name": "Nitrofurantoin", "product_id": "69238-2512_87af7ed1-6ae7-4eaf-ab35-d46d07549450", "dosage_form": "SUSPENSION", "pharm_class": ["Nitrofuran Antibacterial [EPC]", "Nitrofurans [CS]"], "product_ndc": "69238-2512", "generic_name": "Nitrofurantoin", "labeler_name": "Amneal Pharmaceuticals NY LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nitrofurantoin", "active_ingredients": [{"name": "NITROFURANTOIN", "strength": "25 mg/5mL"}], "application_number": "ANDA201679", "marketing_category": "ANDA", "marketing_start_date": "20210531", "listing_expiration_date": "20261231"}