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
71205-424
Product ID
71205-424_d8e60aa5-76e2-4c27-9f03-f6a188be7079
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210000
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
71205424
Hyphenated Format
71205-424
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
ANDA210000 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 1 BLISTER PACK in 1 CARTON (71205-424-06) / 6 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": "d8e60aa5-76e2-4c27-9f03-f6a188be7079", "openfda": {"upc": ["0371205424060"], "unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["99ca0089-14a9-446d-8807-253ad5be3efa"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "1 BLISTER PACK in 1 CARTON (71205-424-06) / 6 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "71205-424-06", "marketing_start_date": "20200311"}], "brand_name": "Azithromycin", "product_id": "71205-424_d8e60aa5-76e2-4c27-9f03-f6a188be7079", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "71205-424", "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": "ANDA210000", "marketing_category": "ANDA", "marketing_start_date": "20190312", "listing_expiration_date": "20261231"}