metronidazole
Generic: metronidazole
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
metronidazole
Generic Name
metronidazole
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
TABLET
Routes
Active Ingredients
metronidazole 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
72789-007
Product ID
72789-007_4030e823-df78-74d4-e063-6394a90ac806
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA079067
Listing Expiration
2026-12-31
Marketing Start
2016-12-01
Pharmacologic Class
Established (EPC)
Chemical Structure
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
72789007
Hyphenated Format
72789-007
Supplemental Identifiers
RxCUI
UPC
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
ANDA079067 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 4 TABLET in 1 BOTTLE, PLASTIC (72789-007-04)
- 6 TABLET in 1 BOTTLE, PLASTIC (72789-007-06)
- 9 TABLET in 1 BOTTLE, PLASTIC (72789-007-09)
- 14 TABLET in 1 BOTTLE, PLASTIC (72789-007-14)
- 21 TABLET in 1 BOTTLE, PLASTIC (72789-007-21)
- 28 TABLET in 1 BOTTLE, PLASTIC (72789-007-28)
- 30 TABLET in 1 BOTTLE, PLASTIC (72789-007-30)
- 1 TABLET in 1 BOTTLE, PLASTIC (72789-007-79)
Packages (8)
72789-007-04
4 TABLET in 1 BOTTLE, PLASTIC (72789-007-04)
72789-007-06
6 TABLET in 1 BOTTLE, PLASTIC (72789-007-06)
72789-007-09
9 TABLET in 1 BOTTLE, PLASTIC (72789-007-09)
72789-007-14
14 TABLET in 1 BOTTLE, PLASTIC (72789-007-14)
72789-007-21
21 TABLET in 1 BOTTLE, PLASTIC (72789-007-21)
72789-007-28
28 TABLET in 1 BOTTLE, PLASTIC (72789-007-28)
72789-007-30
30 TABLET in 1 BOTTLE, PLASTIC (72789-007-30)
72789-007-79
1 TABLET in 1 BOTTLE, PLASTIC (72789-007-79)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4030e823-df78-74d4-e063-6394a90ac806", "openfda": {"nui": ["N0000175435", "M0014907"], "upc": ["0372789007144"], "unii": ["140QMO216E"], "rxcui": ["311681"], "spl_set_id": ["aea4e2a1-2089-40dc-9eee-deaab4f21397"], "pharm_class_cs": ["Nitroimidazoles [CS]"], "pharm_class_epc": ["Nitroimidazole Antimicrobial [EPC]"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET in 1 BOTTLE, PLASTIC (72789-007-04)", "package_ndc": "72789-007-04", "marketing_start_date": "20191216"}, {"sample": false, "description": "6 TABLET in 1 BOTTLE, PLASTIC (72789-007-06)", "package_ndc": "72789-007-06", "marketing_start_date": "20231030"}, {"sample": false, "description": "9 TABLET in 1 BOTTLE, PLASTIC (72789-007-09)", "package_ndc": "72789-007-09", "marketing_start_date": "20191009"}, {"sample": false, "description": "14 TABLET in 1 BOTTLE, PLASTIC (72789-007-14)", "package_ndc": "72789-007-14", "marketing_start_date": "20190913"}, {"sample": false, "description": "21 TABLET in 1 BOTTLE, PLASTIC (72789-007-21)", "package_ndc": "72789-007-21", "marketing_start_date": "20190926"}, {"sample": false, "description": "28 TABLET in 1 BOTTLE, PLASTIC (72789-007-28)", "package_ndc": "72789-007-28", "marketing_start_date": "20200604"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE, PLASTIC (72789-007-30)", "package_ndc": "72789-007-30", "marketing_start_date": "20191121"}, {"sample": false, "description": "1 TABLET in 1 BOTTLE, PLASTIC (72789-007-79)", "package_ndc": "72789-007-79", "marketing_start_date": "20191107"}], "brand_name": "Metronidazole", "product_id": "72789-007_4030e823-df78-74d4-e063-6394a90ac806", "dosage_form": "TABLET", "pharm_class": ["Nitroimidazole Antimicrobial [EPC]", "Nitroimidazoles [CS]"], "product_ndc": "72789-007", "generic_name": "Metronidazole", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Metronidazole", "active_ingredients": [{"name": "METRONIDAZOLE", "strength": "500 mg/1"}], "application_number": "ANDA079067", "marketing_category": "ANDA", "marketing_start_date": "20161201", "listing_expiration_date": "20261231"}