azithromycin

Generic: azithromycin

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name azithromycin
Generic Name azithromycin
Labeler remedyrepack inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

azithromycin dihydrate 500 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3254
Product ID 70518-3254_3cd136df-2496-62e3-e063-6294a90ad73f
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211792
Listing Expiration 2026-12-31
Marketing Start 2021-10-23

Pharmacologic Class

Classes
macrolide antimicrobial [epc] macrolides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183254
Hyphenated Format 70518-3254

Supplemental Identifiers

RxCUI
248656
UNII
5FD1131I7S

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 ANDA211792 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3254-0)
  • 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3254-1)
  • 2 POUCH in 1 BOX (70518-3254-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-3254-3)
  • 3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3254-4)
source: ndc

Packages (4)

70518-3254-0 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3254-0) 70518-3254-1 2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3254-1) 70518-3254-2 2 POUCH in 1 BOX (70518-3254-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-3254-3) 70518-3254-4 3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3254-4)

Ingredients (1)

azithromycin dihydrate (500 mg/1)

Linked Drug Pages (1)

Azithromycin ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3cd136df-2496-62e3-e063-6294a90ad73f", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["614cc2a4-3fc7-455d-9e8a-212c496f0fbf"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3254-0)", "package_ndc": "70518-3254-0", "marketing_start_date": "20211023"}, {"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3254-1)", "package_ndc": "70518-3254-1", "marketing_start_date": "20220114"}, {"sample": false, "description": "2 POUCH in 1 BOX (70518-3254-2)  / 1 TABLET, FILM COATED in 1 POUCH (70518-3254-3)", "package_ndc": "70518-3254-2", "marketing_start_date": "20220210"}, {"sample": false, "description": "3 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3254-4)", "package_ndc": "70518-3254-4", "marketing_start_date": "20220510"}], "brand_name": "Azithromycin", "product_id": "70518-3254_3cd136df-2496-62e3-e063-6294a90ad73f", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70518-3254", "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": "ANDA211792", "marketing_category": "ANDA", "marketing_start_date": "20211023", "listing_expiration_date": "20261231"}