azithromycin dihydrate

Generic: azithromycin dihydrate

Labeler: pd-rx pharmaceuticals, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

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

azithromycin dihydrate 250 mg/1

Manufacturer
PD-Rx Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 72789-081
Product ID 72789-081_31442118-2505-0be0-e063-6294a90a12d1
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA208250
Marketing Start 2019-07-01
Marketing End 2026-11-30

Pharmacologic Class

Classes
macrolide antimicrobial [epc] macrolides [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 72789081
Hyphenated Format 72789-081

Supplemental Identifiers

RxCUI
308460
UPC
0372789081045
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, PLASTIC (72789-081-04)
source: ndc

Packages (1)

72789-081-04 4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-081-04)

Ingredients (1)

azithromycin dihydrate (250 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": "31442118-2505-0be0-e063-6294a90a12d1", "openfda": {"upc": ["0372789081045"], "unii": ["5FD1131I7S"], "rxcui": ["308460"], "spl_set_id": ["e9800bbe-e8bf-4689-a8a5-dc23b5d2ee56"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "4 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-081-04)", "package_ndc": "72789-081-04", "marketing_end_date": "20261130", "marketing_start_date": "20200507"}], "brand_name": "Azithromycin Dihydrate", "product_id": "72789-081_31442118-2505-0be0-e063-6294a90a12d1", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "72789-081", "generic_name": "Azithromycin Dihydrate", "labeler_name": "PD-Rx 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_end_date": "20261130", "marketing_start_date": "20190701"}