azithromycin

Generic: azithromycin

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

Drug Facts

Product Profile

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

azithromycin dihydrate 250 mg/1

Manufacturer
DIRECT RX

Identifiers & Regulatory

Product NDC 72189-093
Product ID 72189-093_26f851bf-1b84-d000-e063-6394a90a079c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210000
Listing Expiration 2026-12-31
Marketing Start 2020-05-15

Pharmacologic Class

Classes
macrolide antimicrobial [epc] macrolides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72189093
Hyphenated Format 72189-093

Supplemental Identifiers

RxCUI
248656 308460 749780 749783
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 (72189-093-06)
source: ndc

Packages (1)

72189-093-06 6 TABLET, FILM COATED in 1 BLISTER PACK (72189-093-06)

Ingredients (1)

azithromycin dihydrate (250 mg/1)

Linked Drug Pages (1)

AZITHROMYCIN, AZITHROMYCIN DIHYDRATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "26f851bf-1b84-d000-e063-6394a90a079c", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["248656", "308460", "749780", "749783"], "spl_set_id": ["a5b4092d-ab72-f5d1-e053-2995a90ac582"], "manufacturer_name": ["DIRECT RX"]}, "finished": true, "packaging": [{"sample": false, "description": "6 TABLET, FILM COATED in 1 BLISTER PACK (72189-093-06)", "package_ndc": "72189-093-06", "marketing_start_date": "20200515"}], "brand_name": "AZITHROMYCIN", "product_id": "72189-093_26f851bf-1b84-d000-e063-6394a90a079c", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "72189-093", "generic_name": "AZITHROMYCIN", "labeler_name": "DIRECT 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": "20200515", "listing_expiration_date": "20261231"}