Package 70436-228-49

Brand: azithromycin dihydrate

Generic: azithromycin dihydrate
NDC Package

Package Facts

Identity

Package NDC 70436-228-49
Digits Only 7043622849
Product NDC 70436-228
Description

1 BOTTLE in 1 CARTON (70436-228-49) / 22.5 mL in 1 BOTTLE

Marketing

Marketing Status
Marketed Since 2024-06-07
Brand azithromycin dihydrate
Generic azithromycin dihydrate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "32f66ed6-7a90-559b-e063-6394a90aaf93", "openfda": {"unii": ["5FD1131I7S"], "rxcui": ["141963", "308459"], "spl_set_id": ["33d4ac05-b564-440c-971d-b78590dd2c32"], "manufacturer_name": ["Slate Run Pharmaceuticals, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 BOTTLE in 1 CARTON (70436-228-49)  / 22.5 mL in 1 BOTTLE", "package_ndc": "70436-228-49", "marketing_start_date": "20240607"}], "brand_name": "azithromycin dihydrate", "product_id": "70436-228_32f66ed6-7a90-559b-e063-6394a90aaf93", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "70436-228", "generic_name": "azithromycin dihydrate", "labeler_name": "Slate Run Pharmaceuticals, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "azithromycin dihydrate", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "200 mg/5mL"}], "application_number": "ANDA217036", "marketing_category": "ANDA", "marketing_start_date": "20240101", "listing_expiration_date": "20261231"}