Metronidazole

Generic: Metronidazole

Labeler: REMEDYREPACK INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Metronidazole
Generic Name Metronidazole
Labeler REMEDYREPACK INC.
Dosage Form TABLET
Routes
ORAL
Active Ingredients

METRONIDAZOLE 500 mg/1

Identifiers & Regulatory

Product NDC 70518-3110
Product ID 70518-3110_3e71c201-a393-b7eb-e063-6294a90a317e
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203974
Listing Expiration 2026-12-31
Marketing Start 2021-06-03

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183110
Hyphenated Format 70518-3110

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 14 TABLET in 1 BOTTLE, PLASTIC (70518-3110-5)
  • 4 TABLET in 1 BOTTLE, PLASTIC (70518-3110-6)
  • 30 TABLET in 1 BLISTER PACK (70518-3110-7)
source: ndc

Packages (3)

70518-3110-5 14 TABLET in 1 BOTTLE, PLASTIC (70518-3110-5) 70518-3110-6 4 TABLET in 1 BOTTLE, PLASTIC (70518-3110-6) 70518-3110-7 30 TABLET in 1 BLISTER PACK (70518-3110-7)

Ingredients (1)

METRONIDAZOLE (500 mg/1)

Linked Drug Pages (1)

Metronidazole ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3e71c201-a393-b7eb-e063-6294a90a317e", "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"}, {"sample": false, "description": "4 TABLET in 1 BOTTLE, PLASTIC (70518-3110-6)", "package_ndc": "70518-3110-6", "marketing_start_date": "20241125"}, {"sample": false, "description": "30 TABLET in 1 BLISTER PACK (70518-3110-7)", "package_ndc": "70518-3110-7", "marketing_start_date": "20250108"}], "brand_name": "Metronidazole", "product_id": "70518-3110_3e71c201-a393-b7eb-e063-6294a90a317e", "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": "20261231"}