azithromycin
Generic: azithromycin
Labeler: nucare pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
azithromycin
Generic Name
azithromycin
Labeler
nucare pharmaceuticals, inc.
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
azithromycin monohydrate 200 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
68071-3897
Product ID
68071-3897_3f7c742b-a360-bef8-e063-6294a90a93ed
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA207531
Listing Expiration
2026-12-31
Marketing Start
2018-04-10
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
680713897
Hyphenated Format
68071-3897
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
ANDA207531 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 200 mg/5mL
Packaging
- 22.5 mL in 1 BOTTLE, PLASTIC (68071-3897-2)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "3f7c742b-a360-bef8-e063-6294a90a93ed", "openfda": {"upc": ["0368071389722"], "unii": ["JTE4MNN1MD"], "rxcui": ["141963"], "spl_set_id": ["3f7c7421-411d-c04e-e063-6394a90a4aa0"], "manufacturer_name": ["NuCare Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "22.5 mL in 1 BOTTLE, PLASTIC (68071-3897-2)", "package_ndc": "68071-3897-2", "marketing_start_date": "20250923"}], "brand_name": "AZITHROMYCIN", "product_id": "68071-3897_3f7c742b-a360-bef8-e063-6294a90a93ed", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68071-3897", "generic_name": "azithromycin", "labeler_name": "NuCare Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "AZITHROMYCIN", "active_ingredients": [{"name": "AZITHROMYCIN MONOHYDRATE", "strength": "200 mg/5mL"}], "application_number": "ANDA207531", "marketing_category": "ANDA", "marketing_start_date": "20180410", "listing_expiration_date": "20261231"}