azithromycin dihydrate
Generic: azithromycin dihydrate
Labeler: avpakDrug Facts
Product Profile
Brand Name
azithromycin dihydrate
Generic Name
azithromycin dihydrate
Labeler
avpak
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
azithromycin dihydrate 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
50268-074
Product ID
50268-074_47e22fe1-c6d6-576b-e063-6394a90a98e6
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208250
Listing Expiration
2027-12-31
Marketing Start
2020-12-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
50268074
Hyphenated Format
50268-074
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 dihydrate (source: ndc)
Generic Name
azithromycin dihydrate (source: ndc)
Application Number
ANDA208250 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 50 BLISTER PACK in 1 BOX (50268-074-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-074-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "47e22fe1-c6d6-576b-e063-6394a90a98e6", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656", "308460"], "spl_set_id": ["b635019e-7fd4-7f9e-e053-2a95a90a388c"], "manufacturer_name": ["AvPAK"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 BOX (50268-074-15) / 1 TABLET, FILM COATED in 1 BLISTER PACK (50268-074-11)", "package_ndc": "50268-074-15", "marketing_start_date": "20210826"}], "brand_name": "Azithromycin Dihydrate", "product_id": "50268-074_47e22fe1-c6d6-576b-e063-6394a90a98e6", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "50268-074", "generic_name": "Azithromycin Dihydrate", "labeler_name": "AvPAK", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA208250", "marketing_category": "ANDA", "marketing_start_date": "20201211", "listing_expiration_date": "20271231"}