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 TABLET, FILM COATED
Routes
ORAL
Active Ingredients

azithromycin dihydrate 500 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

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
macrolide antimicrobial [epc] macrolides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680712297
Hyphenated Format 68071-2297

Supplemental Identifiers

RxCUI
248656
UPC
0368071229721
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 ANDA210001 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 500 mg/1
source: ndc
Packaging
  • 2 TABLET, FILM COATED in 1 BOTTLE (68071-2297-2)
source: ndc

Packages (1)

Ingredients (1)

azithromycin dihydrate (500 mg/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"}