azithromycin dihydrate

Generic: azithromycin dihydrate

Labeler: nucare pharmaceuticals inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name azithromycin dihydrate
Generic Name azithromycin dihydrate
Labeler nucare pharmaceuticals inc.
Dosage Form TABLET, FILM COATED
Routes
ORAL
Active Ingredients

azithromycin dihydrate 250 mg/1

Manufacturer
NuCare Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 68071-3715
Product ID 68071-3715_2a32433c-0956-9672-e063-6394a90a1ac3
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208250
Listing Expiration 2026-12-31
Marketing Start 2024-02-15

Pharmacologic Class

Classes
macrolide antimicrobial [epc] macrolides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680713715
Hyphenated Format 68071-3715

Supplemental Identifiers

RxCUI
308460
UPC
0368071371543
UNII
5FD1131I7S

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 250 mg/1
source: ndc
Packaging
  • 4 TABLET, FILM COATED in 1 BOTTLE (68071-3715-4)
source: ndc

Packages (1)

Ingredients (1)

azithromycin dihydrate (250 mg/1)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2a32433c-0956-9672-e063-6394a90a1ac3", "openfda": {"upc": ["0368071371543"], "unii": ["5FD1131I7S"], "rxcui": ["308460"], "spl_set_id": ["258dd3c5-dce9-7483-e063-6294a90a4043"], "manufacturer_name": ["NuCare Pharmaceuticals Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE (68071-3715-4)", "package_ndc": "68071-3715-4", "marketing_start_date": "20241028"}], "brand_name": "Azithromycin Dihydrate", "product_id": "68071-3715_2a32433c-0956-9672-e063-6394a90a1ac3", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68071-3715", "generic_name": "Azithromycin Dihydrate", "labeler_name": "NuCare Pharmaceuticals Inc.", "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": "20240215", "listing_expiration_date": "20261231"}