azithromycin
Generic: azithromycin
Labeler: avkareDrug Facts
Product Profile
Brand Name
azithromycin
Generic Name
azithromycin
Labeler
avkare
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
azithromycin monohydrate 600 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
42291-044
Product ID
42291-044_484c1370-43ba-a9a6-e063-6294a90ab468
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065218
Listing Expiration
2027-12-31
Marketing Start
2024-04-24
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
42291044
Hyphenated Format
42291-044
Supplemental Identifiers
RxCUI
UNII
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 (42291-044-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "484c1370-43ba-a9a6-e063-6294a90ab468", "openfda": {"unii": ["JTE4MNN1MD"], "rxcui": ["204844"], "spl_set_id": ["16da30a2-d11c-7e8c-e063-6294a90a62e3"], "manufacturer_name": ["AvKARE"]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (42291-044-30)", "package_ndc": "42291-044-30", "marketing_start_date": "20240424"}], "brand_name": "Azithromycin", "product_id": "42291-044_484c1370-43ba-a9a6-e063-6294a90ab468", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "42291-044", "generic_name": "Azithromycin", "labeler_name": "AvKARE", "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": "20240424", "listing_expiration_date": "20271231"}