azithromycin
Generic: azithromycin
Labeler: teva pharmaceuticals usa, inc.Drug Facts
Product Profile
Brand Name
azithromycin
Generic Name
azithromycin
Labeler
teva pharmaceuticals usa, inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
azithromycin monohydrate 600 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50111-789
Product ID
50111-789_d6a6e6e8-3842-49a7-883b-82aa0916f3c7
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065218
Listing Expiration
2026-12-31
Marketing Start
2005-12-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50111789
Hyphenated Format
50111-789
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
azithromycin (source: ndc)
Generic Name
azithromycin (source: ndc)
Application Number
ANDA065218 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 600 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BOTTLE (50111-789-10)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "d6a6e6e8-3842-49a7-883b-82aa0916f3c7", "openfda": {"unii": ["JTE4MNN1MD"], "rxcui": ["204844"], "spl_set_id": ["ac549022-4d7f-4c9f-9244-1a2df9a27276"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (50111-789-10)", "package_ndc": "50111-789-10", "marketing_start_date": "20051201"}], "brand_name": "Azithromycin", "product_id": "50111-789_d6a6e6e8-3842-49a7-883b-82aa0916f3c7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "50111-789", "generic_name": "Azithromycin", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN MONOHYDRATE", "strength": "600 mg/1"}], "application_number": "ANDA065218", "marketing_category": "ANDA", "marketing_start_date": "20051201", "listing_expiration_date": "20261231"}