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 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-0013
Product ID
70518-0013_47d1f6c1-c0b2-b1cc-e063-6294a90a9ef2
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA070027
Listing Expiration
2027-12-31
Marketing Start
2016-11-23
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705180013
Hyphenated Format
70518-0013
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
ANDA070027 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 28 TABLET in 1 BOTTLE, PLASTIC (70518-0013-0)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47d1f6c1-c0b2-b1cc-e063-6294a90a9ef2", "openfda": {"nui": ["N0000175435", "M0014907"], "unii": ["140QMO216E"], "rxcui": ["314106"], "spl_set_id": ["ca450fad-0513-4c45-8ea0-1f46bcbf6a36"], "pharm_class_cs": ["Nitroimidazoles [CS]"], "pharm_class_epc": ["Nitroimidazole Antimicrobial [EPC]"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "28 TABLET in 1 BOTTLE, PLASTIC (70518-0013-0)", "package_ndc": "70518-0013-0", "marketing_start_date": "20161123"}], "brand_name": "Metronidazole", "product_id": "70518-0013_47d1f6c1-c0b2-b1cc-e063-6294a90a9ef2", "dosage_form": "TABLET", "pharm_class": ["Nitroimidazole Antimicrobial [EPC]", "Nitroimidazoles [CS]"], "product_ndc": "70518-0013", "generic_name": "Metronidazole", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metronidazole", "active_ingredients": [{"name": "METRONIDAZOLE", "strength": "250 mg/1"}], "application_number": "ANDA070027", "marketing_category": "ANDA", "marketing_start_date": "20161123", "listing_expiration_date": "20271231"}