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 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-503
Product ID
71205-503_31df881c-4b9b-4717-8f76-98b6ca8be644
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210001
Listing Expiration
2026-12-31
Marketing Start
2019-03-12
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205503
Hyphenated Format
71205-503
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
ANDA210001 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 500 mg/1
Packaging
- 1 BLISTER PACK in 1 BAG (71205-503-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "31df881c-4b9b-4717-8f76-98b6ca8be644", "openfda": {"upc": ["0371205503031"], "unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["34e6364a-ac3d-434e-a90c-cb13ebcf7983"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 BAG (71205-503-03) / 3 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "71205-503-03", "marketing_start_date": "20210226"}], "brand_name": "Azithromycin", "product_id": "71205-503_31df881c-4b9b-4717-8f76-98b6ca8be644", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "71205-503", "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": "ANDA210001", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}