azithromycin
Generic: azithromycin
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
azithromycin
Generic Name
azithromycin
Labeler
remedyrepack inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
azithromycin dihydrate 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-3169
Product ID
70518-3169_46522e5d-73de-53ad-e063-6294a90ad05a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210001
Listing Expiration
2026-12-31
Marketing Start
2021-07-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705183169
Hyphenated Format
70518-3169
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
ANDA210001 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3169-1)
- 2 POUCH in 1 BOX (70518-3169-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-3169-4)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "46522e5d-73de-53ad-e063-6294a90ad05a", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["309652c7-e8a9-4b10-b88a-8812212f7ad3"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3169-1)", "package_ndc": "70518-3169-1", "marketing_start_date": "20240426"}, {"sample": false, "description": "2 POUCH in 1 BOX (70518-3169-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-3169-4)", "package_ndc": "70518-3169-3", "marketing_start_date": "20240913"}], "brand_name": "Azithromycin", "product_id": "70518-3169_46522e5d-73de-53ad-e063-6294a90ad05a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70518-3169", "generic_name": "Azithromycin", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA210001", "marketing_category": "ANDA", "marketing_start_date": "20210722", "listing_expiration_date": "20261231"}