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 500 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-3661
Product ID 68071-3661_21c64584-eb85-869f-e063-6394a90a2a30
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208249
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 680713661
Hyphenated Format 68071-3661

Supplemental Identifiers

RxCUI
248656
UPC
0368071366129
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 ANDA208249 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 2 TABLET, FILM COATED in 1 BOTTLE (68071-3661-2)
  • 6 TABLET, FILM COATED in 1 BOTTLE (68071-3661-6)
source: ndc

Packages (2)

68071-3661-2 2 TABLET, FILM COATED in 1 BOTTLE (68071-3661-2) 68071-3661-6 6 TABLET, FILM COATED in 1 BOTTLE (68071-3661-6)

Ingredients (1)

azithromycin dihydrate (500 mg/1)

Linked Drug Pages (1)

Azithromycin Dihydrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "21c64584-eb85-869f-e063-6394a90a2a30", "openfda": {"upc": ["0368071366129"], "unii": ["5FD1131I7S"], "rxcui": ["248656"], "spl_set_id": ["21c67de0-3a4e-caab-e063-6394a90ae3cd"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "2 TABLET, FILM COATED in 1 BOTTLE (68071-3661-2)", "package_ndc": "68071-3661-2", "marketing_start_date": "20240910"}, {"sample": false, "description": "6 TABLET, FILM COATED in 1 BOTTLE (68071-3661-6)", "package_ndc": "68071-3661-6", "marketing_start_date": "20240910"}], "brand_name": "Azithromycin Dihydrate", "product_id": "68071-3661_21c64584-eb85-869f-e063-6394a90a2a30", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68071-3661", "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": "500 mg/1"}], "application_number": "ANDA208249", "marketing_category": "ANDA", "marketing_start_date": "20240215", "listing_expiration_date": "20261231"}