azithromycin

Generic: azithromycin

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

Drug Facts

Product Profile

Brand Name azithromycin
Generic Name azithromycin
Labeler nucare pharmaceuticals,inc.
Dosage Form POWDER, FOR SUSPENSION
Routes
ORAL
Active Ingredients

azithromycin dihydrate 200 mg/5mL

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-4779
Product ID 68071-4779_1adc1010-cc6d-31f2-e063-6394a90a64c6
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA211147
Listing Expiration 2026-12-31
Marketing Start 2018-08-06

Pharmacologic Class

Classes
macrolide antimicrobial [epc] macrolides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680714779
Hyphenated Format 68071-4779

Supplemental Identifiers

RxCUI
141963
UPC
0368071477931
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 (source: ndc)
Generic Name azithromycin (source: ndc)
Application Number ANDA211147 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 200 mg/5mL
source: ndc
Packaging
  • 30 mL in 1 BOTTLE (68071-4779-3)
source: ndc

Packages (1)

Ingredients (1)

azithromycin dihydrate (200 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "1adc1010-cc6d-31f2-e063-6394a90a64c6", "openfda": {"upc": ["0368071477931"], "unii": ["5FD1131I7S"], "rxcui": ["141963"], "spl_set_id": ["826f9c07-8eb9-a128-e053-2991aa0ad654"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 mL in 1 BOTTLE (68071-4779-3)", "package_ndc": "68071-4779-3", "marketing_start_date": "20190221"}], "brand_name": "Azithromycin", "product_id": "68071-4779_1adc1010-cc6d-31f2-e063-6394a90a64c6", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "68071-4779", "generic_name": "Azithromycin", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "200 mg/5mL"}], "application_number": "ANDA211147", "marketing_category": "ANDA", "marketing_start_date": "20180806", "listing_expiration_date": "20261231"}