azithromycin

Generic: azithromycin

Labeler: doc rx
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name azithromycin
Generic Name azithromycin
Labeler doc rx
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

azithromycin dihydrate 250 mg/1

Manufacturer
Doc Rx

Identifiers & Regulatory

Product NDC 69306-250
Product ID 69306-250_c479da04-f3f7-fa5f-e053-2995a90a9ef8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210000
Listing Expiration 2026-12-31
Marketing Start 2019-03-12

Pharmacologic Class

Classes
macrolide antimicrobial [epc] macrolides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 69306250
Hyphenated Format 69306-250

Supplemental Identifiers

RxCUI
308460 749783
UPC
0369306250060
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 ANDA210000 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 6 TABLET, FILM COATED in 1 BLISTER PACK (69306-250-06)
source: ndc

Packages (1)

69306-250-06 6 TABLET, FILM COATED in 1 BLISTER PACK (69306-250-06)

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": "c479da04-f3f7-fa5f-e053-2995a90a9ef8", "openfda": {"upc": ["0369306250060"], "unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["90ff7cfc-73c9-4d77-83df-c05cfbbbbecd"], "manufacturer_name": ["Doc Rx"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BLISTER PACK (69306-250-06)", "package_ndc": "69306-250-06", "marketing_start_date": "20200411"}], "brand_name": "Azithromycin", "product_id": "69306-250_c479da04-f3f7-fa5f-e053-2995a90a9ef8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "69306-250", "generic_name": "Azithromycin", "labeler_name": "Doc Rx", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA210000", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}