azithromycin
Generic: azithromycin
Labeler: teva pharmaceuticals usa, inc.Drug Facts
Product Profile
Brand Name
azithromycin
Generic Name
azithromycin
Labeler
teva pharmaceuticals usa, inc.
Dosage Form
POWDER, FOR SUSPENSION
Routes
Active Ingredients
azithromycin monohydrate 100 mg/5mL
Manufacturer
Identifiers & Regulatory
Product NDC
0093-2027
Product ID
0093-2027_cce27cc7-6d9a-496a-8989-41323c834241
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA065246
Listing Expiration
2026-12-31
Marketing Start
2010-12-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00932027
Hyphenated Format
0093-2027
Supplemental Identifiers
RxCUI
UNII
Packaging Origin
Original Packager
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
ANDA065246 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 100 mg/5mL
Packaging
- 15 mL in 1 BOTTLE (0093-2027-23)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "cce27cc7-6d9a-496a-8989-41323c834241", "openfda": {"unii": ["JTE4MNN1MD"], "rxcui": ["141963", "308459"], "spl_set_id": ["3209b147-11ce-4eeb-8427-5f8e6fb2c83d"], "manufacturer_name": ["Teva Pharmaceuticals USA, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "15 mL in 1 BOTTLE (0093-2027-23)", "package_ndc": "0093-2027-23", "marketing_start_date": "20101228"}], "brand_name": "Azithromycin", "product_id": "0093-2027_cce27cc7-6d9a-496a-8989-41323c834241", "dosage_form": "POWDER, FOR SUSPENSION", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "0093-2027", "generic_name": "Azithromycin", "labeler_name": "Teva Pharmaceuticals USA, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Azithromycin", "active_ingredients": [{"name": "AZITHROMYCIN MONOHYDRATE", "strength": "100 mg/5mL"}], "application_number": "ANDA065246", "marketing_category": "ANDA", "marketing_start_date": "20101228", "listing_expiration_date": "20261231"}