AstraZeneca Unclassified
FDA Approved Drugs
AstraZeneca Unclassified
FDA Approved Drugs Database
FDA approved drug product records including application numbers, product numbers, drug names, active ingredients, dosage forms, strengths, approval dates and regulatory status.
- Total Records 15
- Latest Approval Date -
- Data Source FDA
- First Approval Date -
Company Overview
Company
AstraZeneca Unclassified
Country
United Kingdom
Website
Social Profiles
Company Snapshot
AstraZeneca Unclassified
2 Kingdom Street, Paddington, London W2 6BD
United Kingdom
www.astrazeneca.com/ Russell.Gantt@astrazeneca.com View on MapFDA Approved Drug Records ( 15 records )
Drug Name
ARIMIDEX
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
-
Active Ingredient
ANASTROZOLE
Application Number
22214
Product Number
1
Dosage Form
-
Strength
1MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
BEYFORTUS
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
-
Active Ingredient
NIRSEVIMAB-ALIP
Application Number
761328
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
BEYFORTUS
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
-
Active Ingredient
NIRSEVIMAB-ALIP
Application Number
761328
Product Number
2
Dosage Form
-
Strength
100MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CASODEX
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
-
Active Ingredient
BICALUTAMIDE
Application Number
22310
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
FASENRA
Product Number
1
Dosage Form
-
Strength
30MG/ML
Approval Date
-
Active Ingredient
BENRALIZUMAB
Application Number
761070
Product Number
1
Dosage Form
-
Strength
30MG/ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
IMJUDO
Product Number
1
Dosage Form
-
Strength
25MG/1.25ML(20MG/ML)
Approval Date
-
Active Ingredient
TREMELIMUMAB-ACTL
Application Number
761270
Product Number
1
Dosage Form
-
Strength
25MG/1.25ML(20MG/ML)
Approval Date
-
Regulatory Status
Unclassified
Drug Name
IMJUDO
Product Number
2
Dosage Form
-
Strength
300MG/15ML(20MG/ML)
Approval Date
-
Active Ingredient
TREMELIMUMAB-ACTL
Application Number
761270
Product Number
2
Dosage Form
-
Strength
300MG/15ML(20MG/ML)
Approval Date
-
Regulatory Status
Unclassified
Drug Name
IMJUDO
Product Number
1
Dosage Form
-
Strength
25MG/1.25ML(20MG/ML)
Approval Date
-
Active Ingredient
TREMELIMUMAB-ACTL
Application Number
761289
Product Number
1
Dosage Form
-
Strength
25MG/1.25ML(20MG/ML)
Approval Date
-
Regulatory Status
Unclassified
Drug Name
IMJUDO
Product Number
2
Dosage Form
-
Strength
300MG/15ML(20MG/ML)
Approval Date
-
Active Ingredient
TREMELIMUMAB-ACTL
Application Number
761289
Product Number
2
Dosage Form
-
Strength
300MG/15ML(20MG/ML)
Approval Date
-
Regulatory Status
Unclassified
Drug Name
KOSELUGO
Product Number
3
Dosage Form
-
Strength
10MG
Approval Date
-
Active Ingredient
SELUMETINIB
Application Number
219943
Product Number
3
Dosage Form
-
Strength
10MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
KOSELUGO
Product Number
4
Dosage Form
-
Strength
25MG
Approval Date
-
Active Ingredient
SELUMETINIB
Application Number
219943
Product Number
4
Dosage Form
-
Strength
25MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
SAPHNELO
Product Number
1
Dosage Form
-
Strength
300MG/2ML(150MG/ML)
Approval Date
-
Active Ingredient
ANIFROLUMAB-FNIA
Application Number
761123
Product Number
1
Dosage Form
-
Strength
300MG/2ML(150MG/ML)
Approval Date
-
Regulatory Status
Unclassified
Drug Name
SAPHNELO
Product Number
1
Dosage Form
-
Strength
300MG/2ML (150MG/ML
Approval Date
-
Active Ingredient
ANIFROLUMAB-FNIA
Application Number
761451
Product Number
1
Dosage Form
-
Strength
300MG/2ML (150MG/ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
SAPHNELO
Product Number
2
Dosage Form
-
Strength
120MG/0.8ML
Approval Date
-
Active Ingredient
ANIFROLUMAB-FNIA
Application Number
761451
Product Number
2
Dosage Form
-
Strength
120MG/0.8ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
TEZSPIRE
Product Number
1
Dosage Form
-
Strength
210MG/1.91ML(110MG/ML)
Approval Date
-
Active Ingredient
TEZEPELUMAB-EKKO
Application Number
761224
Product Number
1
Dosage Form
-
Strength
210MG/1.91ML(110MG/ML)
Approval Date
-
Regulatory Status
Unclassified
Drug Status Breakdown
15 total- Unclassified
Official Source
FDA approved drug data is based on publicly available U.S. Food and Drug Administration Orange Book information.
Visit FDA Orange BookFDA Approved Drug Record Details Preview
Explore important FDA approved drug information available in the records above.
Drug Name
ARIMIDEX
Application Number
22214
Product Number
1
Active Ingredient
ANASTROZOLE
Dosage Form
-
Strength
1MG
FDA Approved Drug Data
Approved drug product information
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