zithromax
Generic: azithromycin dihydrate
Labeler: pfizer laboratories div pfizer incDrug Facts
Product Profile
Brand Name
zithromax
Generic Name
azithromycin dihydrate
Labeler
pfizer laboratories div pfizer inc
Dosage Form
TABLET, FILM COATED
Routes
Active Ingredients
azithromycin dihydrate 250 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0069-3060
Product ID
0069-3060_e15f2173-8700-4392-96a4-8560772b6f8a
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA050711
Listing Expiration
2027-12-31
Marketing Start
1996-07-18
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
00693060
Hyphenated Format
0069-3060
Supplemental Identifiers
RxCUI
UPC
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
zithromax (source: ndc)
Generic Name
azithromycin dihydrate (source: ndc)
Application Number
NDA050711 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 250 mg/1
Packaging
- 3 BLISTER PACK in 1 BOX (0069-3060-75) / 6 TABLET, FILM COATED in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "e15f2173-8700-4392-96a4-8560772b6f8a", "openfda": {"upc": ["0300693060306", "0300693070305"], "unii": ["5FD1131I7S"], "rxcui": ["105260", "141963", "211307", "212446", "226827", "248656", "308459", "308460", "749780", "749783", "750149", "750157"], "spl_set_id": ["db52b91e-79f7-4cc1-9564-f2eee8e31c45"], "manufacturer_name": ["Pfizer Laboratories Div Pfizer Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "3 BLISTER PACK in 1 BOX (0069-3060-75) / 6 TABLET, FILM COATED in 1 BLISTER PACK", "package_ndc": "0069-3060-75", "marketing_start_date": "19960718"}], "brand_name": "Zithromax", "product_id": "0069-3060_e15f2173-8700-4392-96a4-8560772b6f8a", "dosage_form": "TABLET, FILM COATED", "pharm_class": ["Macrolide Antimicrobial [EPC]", "Macrolides [CS]"], "product_ndc": "0069-3060", "generic_name": "azithromycin dihydrate", "labeler_name": "Pfizer Laboratories Div Pfizer Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Zithromax", "active_ingredients": [{"name": "AZITHROMYCIN DIHYDRATE", "strength": "250 mg/1"}], "application_number": "NDA050711", "marketing_category": "NDA", "marketing_start_date": "19960718", "listing_expiration_date": "20271231"}