metronidazole

Generic: metronidazole

Labeler: a-s medication solutions
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name metronidazole
Generic Name metronidazole
Labeler a-s medication solutions
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

metronidazole 500 mg/1

Manufacturer
A-S Medication Solutions

Identifiers & Regulatory

Product NDC 50090-0211
Product ID 50090-0211_94ad2416-78e2-4f6b-9a8f-cd785d90a807
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA203458
Listing Expiration 2026-12-31
Marketing Start 2014-06-01

Pharmacologic Class

Established (EPC)
nitroimidazole antimicrobial [epc]
Chemical Structure
nitroimidazoles [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 500900211
Hyphenated Format 50090-0211

Supplemental Identifiers

RxCUI
311681
UNII
140QMO216E
NUI
N0000175435 M0014907

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 ANDA203458 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 4 TABLET, FILM COATED in 1 BOTTLE (50090-0211-0)
  • 14 TABLET, FILM COATED in 1 BOTTLE (50090-0211-3)
  • 21 TABLET, FILM COATED in 1 BOTTLE (50090-0211-4)
  • 28 TABLET, FILM COATED in 1 BOTTLE (50090-0211-6)
  • 20 TABLET, FILM COATED in 1 BOTTLE (50090-0211-9)
source: ndc

Packages (5)

50090-0211-0 4 TABLET, FILM COATED in 1 BOTTLE (50090-0211-0) 50090-0211-3 14 TABLET, FILM COATED in 1 BOTTLE (50090-0211-3) 50090-0211-4 21 TABLET, FILM COATED in 1 BOTTLE (50090-0211-4) 50090-0211-6 28 TABLET, FILM COATED in 1 BOTTLE (50090-0211-6) 50090-0211-9 20 TABLET, FILM COATED in 1 BOTTLE (50090-0211-9)

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": "94ad2416-78e2-4f6b-9a8f-cd785d90a807", "openfda": {"nui": ["N0000175435", "M0014907"], "unii": ["140QMO216E"], "rxcui": ["311681"], "spl_set_id": ["9a18debb-3bb8-4b23-949b-aaa0f3b62191"], "pharm_class_cs": ["Nitroimidazoles [CS]"], "pharm_class_epc": ["Nitroimidazole Antimicrobial [EPC]"], "manufacturer_name": ["A-S Medication Solutions"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (50090-0211-0)", "package_ndc": "50090-0211-0", "marketing_start_date": "20160621"}, {"sample": false, "description": "14 TABLET, FILM COATED in 1 BOTTLE (50090-0211-3)", "package_ndc": "50090-0211-3", "marketing_start_date": "20141128"}, {"sample": false, "description": "21 TABLET, FILM COATED in 1 BOTTLE (50090-0211-4)", "package_ndc": "50090-0211-4", "marketing_start_date": "20141128"}, {"sample": false, "description": "28 TABLET, FILM COATED in 1 BOTTLE (50090-0211-6)", "package_ndc": "50090-0211-6", "marketing_start_date": "20141128"}, {"sample": false, "description": "20 TABLET, FILM COATED in 1 BOTTLE (50090-0211-9)", "package_ndc": "50090-0211-9", "marketing_start_date": "20141128"}], "brand_name": "Metronidazole", "product_id": "50090-0211_94ad2416-78e2-4f6b-9a8f-cd785d90a807", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Nitroimidazole Antimicrobial [EPC]", "Nitroimidazoles [CS]"], "product_ndc": "50090-0211", "generic_name": "Metronidazole", "labeler_name": "A-S Medication Solutions", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metronidazole", "active_ingredients": [{"name": "METRONIDAZOLE", "strength": "500 mg/1"}], "application_number": "ANDA203458", "marketing_category": "ANDA", "marketing_start_date": "20140601", "listing_expiration_date": "20261231"}