azithromycin

Generic: azithromycin

Labeler: proficient rx lp
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

azithromycin dihydrate 500 mg/1

Manufacturer
Proficient Rx LP

Identifiers & Regulatory

Product NDC 71205-519
Product ID 71205-519_8a140f7c-4dc7-454d-9ff9-473f4306a649
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA207398
Listing Expiration 2026-12-31
Marketing Start 2018-07-05

Pharmacologic Class

Classes
macrolide antimicrobial [epc] macrolides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 71205519
Hyphenated Format 71205-519

Supplemental Identifiers

RxCUI
248656 749780
UPC
0371205519032
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 ANDA207398 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 1 BLISTER PACK in 1 CARTON (71205-519-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK
  • 30 TABLET, FILM COATED in 1 BOTTLE (71205-519-30)
source: ndc

Packages (2)

71205-519-03 1 BLISTER PACK in 1 CARTON (71205-519-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK 71205-519-30 30 TABLET, FILM COATED in 1 BOTTLE (71205-519-30)

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": "8a140f7c-4dc7-454d-9ff9-473f4306a649", "openfda": {"upc": ["0371205519032"], "unii": ["5FD1131I7S"], "rxcui": ["248656", "749780"], "spl_set_id": ["25f2d819-ae38-4061-a897-bbcfce3739bf"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (71205-519-03)  / 3 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "71205-519-03", "marketing_start_date": "20210104"}, {"sample": false, "description": "30 TABLET, FILM COATED in 1 BOTTLE (71205-519-30)", "package_ndc": "71205-519-30", "marketing_start_date": "20210104"}], "brand_name": "Azithromycin", "product_id": "71205-519_8a140f7c-4dc7-454d-9ff9-473f4306a649", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "71205-519", "generic_name": "Azithromycin", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "500 mg/1"}], "application_number": "ANDA207398", "marketing_category": "ANDA", "marketing_start_date": "20180705", "listing_expiration_date": "20261231"}