zithromax

Generic: azithromycin dihydrate

Labeler: redpharm drug
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name zithromax
Generic Name azithromycin dihydrate
Labeler redpharm drug
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

azithromycin dihydrate 250 mg/1

Manufacturer
Redpharm Drug

Identifiers & Regulatory

Product NDC 67296-0020
Product ID 67296-0020_3ddecd2f-ea4c-536f-e063-6294a90a7936
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA050711
Listing Expiration 2026-12-31
Marketing Start 1996-07-18

Pharmacologic Class

Classes
macrolide antimicrobial [epc] macrolides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 672960020
Hyphenated Format 67296-0020

Supplemental Identifiers

RxCUI
212446 308460
UPC
0300693060306 0300693070305
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 zithromax (source: ndc)
Generic Name azithromycin dihydrate (source: ndc)
Application Number NDA050711 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 4 TABLET, FILM COATED in 1 BOTTLE (67296-0020-1)
  • 6 TABLET, FILM COATED in 1 BOTTLE (67296-0020-2)
source: ndc

Packages (2)

67296-0020-1 4 TABLET, FILM COATED in 1 BOTTLE (67296-0020-1) 67296-0020-2 6 TABLET, FILM COATED in 1 BOTTLE (67296-0020-2)

Ingredients (1)

azithromycin dihydrate (250 mg/1)

Linked Drug Pages (1)

Zithromax ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3ddecd2f-ea4c-536f-e063-6294a90a7936", "openfda": {"upc": ["0300693060306", "0300693070305"], "unii": ["5FD1131I7S"], "rxcui": ["212446", "308460"], "spl_set_id": ["3ddecd25-dc32-a2af-e063-6294a90a526d"], "manufacturer_name": ["Redpharm Drug"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (67296-0020-1)", "package_ndc": "67296-0020-1", "marketing_start_date": "19960718"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (67296-0020-2)", "package_ndc": "67296-0020-2", "marketing_start_date": "19960718"}], "brand_name": "Zithromax", "product_id": "67296-0020_3ddecd2f-ea4c-536f-e063-6294a90a7936", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "67296-0020", "generic_name": "azithromycin dihydrate", "labeler_name": "Redpharm Drug", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zithromax", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "NDA050711", "marketing_category": "NDA", "marketing_start_date": "19960718", "listing_expiration_date": "20261231"}