metronidazole
Generic: metronidazole
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
metronidazole
Generic Name
metronidazole
Labeler
remedyrepack inc.
Dosage Form
TABLET
Routes
Active Ingredients
metronidazole 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3110
Product ID
70518-3110_4ab57d98-064d-27f9-e063-6294a90ad62a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA203974
Listing Expiration
2027-12-31
Marketing Start
2021-06-03
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183110
Hyphenated Format
70518-3110
Supplemental Identifiers
RxCUI
UNII
NUI
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
metronidazole (source: ndc)
Generic Name
metronidazole (source: ndc)
Application Number
ANDA203974 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 14 TABLET in 1 BOTTLE, PLASTIC (70518-3110-5)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4ab57d98-064d-27f9-e063-6294a90ad62a", "openfda": {"nui": ["N0000175435", "M0014907"], "unii": ["140QMO216E"], "rxcui": ["311681"], "spl_set_id": ["dc28753c-95ec-4b41-ad77-c4a66698d9db"], "pharm_class_cs": ["Nitroimidazoles [CS]"], "pharm_class_epc": ["Nitroimidazole Antimicrobial [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (70518-3110-5)", "package_ndc": "70518-3110-5", "marketing_start_date": "20240930"}], "brand_name": "Metronidazole", "product_id": "70518-3110_4ab57d98-064d-27f9-e063-6294a90ad62a", "dosage_form": "TABLET", "pharm_class": ["Nitroimidazole Antimicrobial [EPC]", "Nitroimidazoles [CS]"], "product_ndc": "70518-3110", "generic_name": "Metronidazole", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metronidazole", "active_ingredients": [{"name": "METRONIDAZOLE", "strength": "500 mg/1"}], "application_number": "ANDA203974", "marketing_category": "ANDA", "marketing_start_date": "20210603", "listing_expiration_date": "20271231"}