Hetero Drugs Unclassified
FDA Approved Drugs
Hetero Drugs 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 18
- Latest Approval Date -
- Data Source FDA
- First Approval Date -
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Hetero Drugs Unclassified
7-2-A2, Hetero Corporate Industrial Estates, Sanath Nagar Hyderabad,Telangana
India
www.hetero.com/ contact@heterodrugs.com View on MapFDA Approved Drug Records ( 18 records )
Drug Name
AZILSARTAN MEDOXOMIL
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
-
Active Ingredient
AZILSARTAN MEDOXOMIL
Application Number
219062
Product Number
1
Dosage Form
-
Strength
80MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
AZILSARTAN MEDOXOMIL
Product Number
2
Dosage Form
-
Strength
40MG
Approval Date
-
Active Ingredient
AZILSARTAN MEDOXOMIL
Application Number
219062
Product Number
2
Dosage Form
-
Strength
40MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
AZILSARTAN MEDOXOMIL
Product Number
3
Dosage Form
-
Strength
20MG
Approval Date
-
Active Ingredient
AZILSARTAN MEDOXOMIL
Application Number
219062
Product Number
3
Dosage Form
-
Strength
20MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CYCLOPHOSPHAMIDE
Product Number
2
Dosage Form
-
Strength
500MG/2.5ML
Approval Date
-
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
219271
Product Number
2
Dosage Form
-
Strength
500MG/2.5ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
CYCLOPHOSPHAMIDE
Product Number
3
Dosage Form
-
Strength
2000MG/10ML
Approval Date
-
Active Ingredient
CYCLOPHOSPHAMIDE
Application Number
219271
Product Number
3
Dosage Form
-
Strength
2000MG/10ML
Approval Date
-
Regulatory Status
Unclassified
Drug Name
EFAVIRENZ, LAMIVUDINE, AND TENOFOVIR DISOPROXIL FUMARATE
Product Number
1
Dosage Form
-
Strength
600MG;300MG;300MG
Approval Date
-
Active Ingredient
EFAVIRENZ;LAMIVUDINE;TENOFOVIR DISOPROXIL FUMARATE
Application Number
204119
Product Number
1
Dosage Form
-
Strength
600MG;300MG;300MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
ELAGOLIX
Product Number
2
Dosage Form
-
Strength
150MG
Approval Date
-
Active Ingredient
ELAGOLIX
Application Number
217690
Product Number
2
Dosage Form
-
Strength
150MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LAMIVUDINE AND STAVUDINE
Product Number
1
Dosage Form
-
Strength
150MG/30MG
Approval Date
-
Active Ingredient
LAMIVUDINE; STAVUDINE
Application Number
22479
Product Number
1
Dosage Form
-
Strength
150MG/30MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LAMIVUDINE, NEVIRAPINE, AND STAVUDINE
Product Number
1
Dosage Form
-
Strength
150MG; 200MG; 30MG
Approval Date
-
Active Ingredient
LAMIVUDINE; NEVIRAPINE; STAVUDINE
Application Number
200244
Product Number
1
Dosage Form
-
Strength
150MG; 200MG; 30MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LAMIVUDINE, ZIDOVUDINE TABS 150MG/300MG CO-PACKAGED WITH NEVIRAPINE TABS 200MG
Product Number
1
Dosage Form
-
Strength
150MG; 300MG; 200MG
Approval Date
-
Active Ingredient
LAMIVUDINE; ZIDOVUDINE; NEVIRAPINE
Application Number
22356
Product Number
1
Dosage Form
-
Strength
150MG; 300MG; 200MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LAMIVUDINE/TENOFOVIR DISOPROXIL FUMARATE FDC TABS
Product Number
1
Dosage Form
-
Strength
300MG/300MG
Approval Date
-
Active Ingredient
LAMIVUDINE; TENOFOVIR
Application Number
22459
Product Number
1
Dosage Form
-
Strength
300MG/300MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LUMATEPERONE TOSYLATE
Product Number
2
Dosage Form
-
Strength
21MG
Approval Date
-
Active Ingredient
LUMATEPERONE TOSYLATE
Application Number
219142
Product Number
2
Dosage Form
-
Strength
21MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LUMATEPERONE TOSYLATE
Product Number
3
Dosage Form
-
Strength
42MG
Approval Date
-
Active Ingredient
LUMATEPERONE TOSYLATE
Application Number
219142
Product Number
3
Dosage Form
-
Strength
42MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LUMATEPERONE TOSYLATE
Product Number
4
Dosage Form
-
Strength
14MG
Approval Date
-
Active Ingredient
LUMATEPERONE TOSYLATE
Application Number
219142
Product Number
4
Dosage Form
-
Strength
14MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
LUMATEPERONE TOSYLATE
Product Number
5
Dosage Form
-
Strength
28MG
Approval Date
-
Active Ingredient
LUMATEPERONE TOSYLATE
Application Number
219142
Product Number
5
Dosage Form
-
Strength
28MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
SOLRIAMFETOL
Product Number
1
Dosage Form
-
Strength
300MG
Approval Date
-
Active Ingredient
SOLRIAMFETOL
Application Number
218654
Product Number
1
Dosage Form
-
Strength
300MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
SOLRIAMFETOL
Product Number
2
Dosage Form
-
Strength
75MG
Approval Date
-
Active Ingredient
SOLRIAMFETOL
Application Number
218654
Product Number
2
Dosage Form
-
Strength
75MG
Approval Date
-
Regulatory Status
Unclassified
Drug Name
SOLRIAMFETOL
Product Number
3
Dosage Form
-
Strength
150MG
Approval Date
-
Active Ingredient
SOLRIAMFETOL
Application Number
218654
Product Number
3
Dosage Form
-
Strength
150MG
Approval Date
-
Regulatory Status
Unclassified
Drug Status Breakdown
18 total- Unclassified
Official Source
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Drug Name
AZILSARTAN MEDOXOMIL
Application Number
219062
Product Number
1
Active Ingredient
AZILSARTAN MEDOXOMIL
Dosage Form
-
Strength
80MG
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