azithromycin dihydrate
Generic: azithromycin dihydrate
Labeler: proficient rx lpDrug Facts
Product Profile
Brand Name
azithromycin dihydrate
Generic Name
azithromycin dihydrate
Labeler
proficient rx lp
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
azithromycin dihydrate 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
71205-430
Product ID
71205-430_edcedd16-fe45-4edb-a0f8-55d904a59096
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA208250
Listing Expiration
2026-12-31
Marketing Start
2019-07-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
71205430
Hyphenated Format
71205-430
Supplemental Identifiers
RxCUI
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 dihydrate (source: ndc)
Generic Name
azithromycin dihydrate (source: ndc)
Application Number
ANDA208250 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 4 TABLET, FILM COATED in 1 BOTTLE (71205-430-04)
- 1 BLISTER PACK in 1 CARTON (71205-430-06) / 6 TABLET, FILM COATED in 1 BLISTER PACK
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "edcedd16-fe45-4edb-a0f8-55d904a59096", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["308460", "749783"], "spl_set_id": ["8037c6f4-4881-4740-8229-2aee56141cd0"], "manufacturer_name": ["Proficient Rx LP"]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (71205-430-04)", "package_ndc": "71205-430-04", "marketing_start_date": "20201223"}, {"sample": false, "description": "1 BLISTER PACK in 1 CARTON (71205-430-06) / 6 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "71205-430-06", "marketing_start_date": "20200317"}], "brand_name": "Azithromycin Dihydrate", "product_id": "71205-430_edcedd16-fe45-4edb-a0f8-55d904a59096", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "71205-430", "generic_name": "Azithromycin Dihydrate", "labeler_name": "Proficient Rx LP", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin Dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "ANDA208250", "marketing_category": "ANDA", "marketing_start_date": "20190701", "listing_expiration_date": "20261231"}