azithromycin

Generic: azithromycin

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name azithromycin
Generic Name azithromycin
Labeler major pharmaceuticals
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

azithromycin dihydrate 250 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7350
Product ID 0904-7350_7cae275e-abb8-4fad-af20-fa3fdbf095e5
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065398
Listing Expiration 2026-12-31
Marketing Start 2023-05-01

Pharmacologic Class

Classes
macrolide antimicrobial [epc] macrolides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047350
Hyphenated Format 0904-7350

Supplemental Identifiers

RxCUI
248656 308460
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 ANDA065398 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 50 BLISTER PACK in 1 CARTON (0904-7350-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK
  • 100 BLISTER PACK in 1 CARTON (0904-7350-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK
source: ndc

Packages (2)

0904-7350-06 50 BLISTER PACK in 1 CARTON (0904-7350-06) / 1 TABLET, FILM COATED in 1 BLISTER PACK 0904-7350-61 100 BLISTER PACK in 1 CARTON (0904-7350-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK

Ingredients (1)

azithromycin dihydrate (250 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": "7cae275e-abb8-4fad-af20-fa3fdbf095e5", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656", "308460"], "spl_set_id": ["814abe38-da4a-48af-bf4b-2ce04a5aabd1"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "50 BLISTER PACK in 1 CARTON (0904-7350-06)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7350-06", "marketing_start_date": "20230501"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7350-61)  / 1 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0904-7350-61", "marketing_start_date": "20230501"}], "brand_name": "azithromycin", "product_id": "0904-7350_7cae275e-abb8-4fad-af20-fa3fdbf095e5", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "0904-7350", "generic_name": "azithromycin", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA065398", "marketing_category": "ANDA", "marketing_start_date": "20230501", "listing_expiration_date": "20261231"}