azithromycin dihydrate
Generic: azithromycin dihydrate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
azithromycin dihydrate
Generic Name
azithromycin dihydrate
Labeler
remedyrepack inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
azithromycin dihydrate 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4105
Product ID
70518-4105_49ff5d61-b7a0-9f10-e063-6394a90a25fe
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208249
Listing Expiration
2027-12-31
Marketing Start
2024-06-17
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184105
Hyphenated Format
70518-4105
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
ANDA208249 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4105-0)
- 5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4105-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "49ff5d61-b7a0-9f10-e063-6394a90a25fe", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["7711e846-0bb3-486c-8511-f445e264cd98"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4105-0)", "package_ndc": "70518-4105-0", "marketing_start_date": "20240617"}, {"sample": false, "description": "5 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4105-1)", "package_ndc": "70518-4105-1", "marketing_start_date": "20260203"}], "brand_name": "Azithromycin Dihydrate", "product_id": "70518-4105_49ff5d61-b7a0-9f10-e063-6394a90a25fe", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70518-4105", "generic_name": "Azithromycin dihydrate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA208249", "marketing_category": "ANDA", "marketing_start_date": "20240617", "listing_expiration_date": "20271231"}