azithromycin
Generic: azithromycin
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
azithromycin
Generic Name
azithromycin
Labeler
proficient rx lp
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
azithromycin dihydrate 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-645
Product ID
71205-645_8e6754bd-b54c-41db-ae4b-a69b9f8424d8
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065211
Listing Expiration
2026-12-31
Marketing Start
2005-11-14
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205645
Hyphenated Format
71205-645
Supplemental Identifiers
RxCUI
UPC
UNII
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
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 6 DOSE PACK in 1 CARTON (71205-645-06) / 1 TABLET, FILM COATED in 1 DOSE PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "8e6754bd-b54c-41db-ae4b-a69b9f8424d8", "openfda": {"upc": ["0371205645069"], "unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["38942011-f86b-4e42-a4ca-05a70d9dd3d9"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "6 DOSE PACK in 1 CARTON (71205-645-06) / 1 TABLET, FILM COATED in 1 DOSE PACK", "package_ndc": "71205-645-06", "marketing_start_date": "20220318"}], "brand_name": "Azithromycin", "product_id": "71205-645_8e6754bd-b54c-41db-ae4b-a69b9f8424d8", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "71205-645", "generic_name": "Azithromycin", "labeler_name": "Proficient Rx LP", "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"}