Azithromycin

Generic: Azithromycin

Labeler: ASCLEMED USA INC.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Active

Drug Facts

Product Profile

Brand Name Azithromycin
Generic Name Azithromycin
Labeler ASCLEMED USA INC.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

AZITHROMYCIN DIHYDRATE 250 mg/1

Identifiers & Regulatory

Product NDC 76420-404
Product ID 76420-404_37fd3847-b883-06dc-e063-6394a90ad234
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA065211
Listing Expiration 2026-12-31
Marketing Start 2005-11-14

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 76420404
Hyphenated Format 76420-404

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 ANDA065211 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 6 DOSE PACK in 1 CARTON (76420-404-06) / 1 TABLET, FILM COATED in 1 DOSE PACK
source: ndc

Packages (1)

Ingredients (1)

AZITHROMYCIN DIHYDRATE (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "37fd3847-b883-06dc-e063-6394a90ad234", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["4dc2d95d-419d-4401-8f63-68f9287198e6"], "manufacturer_name": ["ASCLEMED USA INC."]}, "finished": true, "packaging": [{"sample": false, "description": "6 DOSE PACK in 1 CARTON (76420-404-06)  / 1 TABLET, FILM COATED in 1 DOSE PACK", "package_ndc": "76420-404-06", "marketing_start_date": "20250618"}], "brand_name": "Azithromycin", "product_id": "76420-404_37fd3847-b883-06dc-e063-6394a90ad234", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "76420-404", "generic_name": "Azithromycin", "labeler_name": "ASCLEMED USA INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA065211", "marketing_category": "ANDA", "marketing_start_date": "20051114", "listing_expiration_date": "20261231"}