azithromycin
Generic: azithromycin
Labeler: nucare pharmaceuticals,inc.Drug Facts
Product Profile
Brand Name
azithromycin
Generic Name
azithromycin
Labeler
nucare pharmaceuticals,inc.
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
azithromycin dihydrate 500 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68071-2297
Product ID
68071-2297_1d784ba4-83f4-0a32-e063-6294a90a63a9
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
680712297
Hyphenated Format
68071-2297
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
- 2 TABLET, FILM COATED in 1 BOTTLE (68071-2297-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1d784ba4-83f4-0a32-e063-6294a90a63a9", "openfda": {"upc": ["0368071229721"], "unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["b43d23c7-1a2e-ce93-e053-2995a90a65a4"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (68071-2297-2)", "package_ndc": "68071-2297-2", "marketing_start_date": "20201116"}], "brand_name": "Azithromycin", "product_id": "68071-2297_1d784ba4-83f4-0a32-e063-6294a90a63a9", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68071-2297", "generic_name": "Azithromycin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "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"}