azithromycin dihydrate

Generic: azithromycin dihydrate

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

Drug Facts

Product Profile

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

azithromycin dihydrate 600 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-4202
Product ID 70518-4202_3ff532ea-01f0-307a-e063-6294a90a2fb7
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207566
Listing Expiration 2026-12-31
Marketing Start 2024-10-02

Pharmacologic Class

Classes
macrolide antimicrobial [epc] macrolides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705184202
Hyphenated Format 70518-4202

Supplemental Identifiers

RxCUI
204844
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 dihydrate (source: ndc)
Generic Name azithromycin dihydrate (source: ndc)
Application Number ANDA207566 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 600 mg/1
source: ndc
Packaging
  • 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4202-0)
source: ndc

Packages (1)

70518-4202-0 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4202-0)

Ingredients (1)

azithromycin dihydrate (600 mg/1)

Linked Drug Pages (1)

Azithromycin Dihydrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ff532ea-01f0-307a-e063-6294a90a2fb7", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["204844"], "spl_set_id": ["0d5129e4-8b94-4a4d-baa9-be0d6b32d714"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4202-0)", "package_ndc": "70518-4202-0", "marketing_start_date": "20241002"}], "brand_name": "Azithromycin Dihydrate", "product_id": "70518-4202_3ff532ea-01f0-307a-e063-6294a90a2fb7", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70518-4202", "generic_name": "Azithromycin dihydrate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "600 mg/1"}], "application_number": "ANDA207566", "marketing_category": "ANDA", "marketing_start_date": "20241002", "listing_expiration_date": "20261231"}