Avanthi Pharma
FDA Approved Drugs
Avanthi Pharma
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 16
- Latest Approval Date Aug 07, 2017
- Data Source FDA
- First Approval Date Mar 06, 2009
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Avanthi Pharma
110 Terry Drive, Suite 100. Newtown, PA 18940
U.S.A
avanthiinc.com/ info@avanthiinc.com View on MapFDA Approved Drug Records ( 16 records )
Drug Name
CHLORPHENIRAMINE MALEATE
Product Number
1
Dosage Form
-
Strength
12MG
Approval Date
2009-05-13
Active Ingredient
CHLORPHENIRAMINE MALEATE
Application Number
40829
Product Number
1
Dosage Form
-
Strength
12MG
Approval Date
2009-05-13
Regulatory Status
OTC
Drug Name
DEXBROMPHENIRAMINE MALEATE AND PSEUDOEPHEDRINE SULFATE
Product Number
1
Dosage Form
-
Strength
6MG;120MG
Approval Date
2013-02-27
Active Ingredient
DEXBROMPHENIRAMINE MALEATE; PSEUDOEPHEDRINE SULFATE
Application Number
78648
Product Number
1
Dosage Form
-
Strength
6MG;120MG
Approval Date
2013-02-27
Regulatory Status
Discontinued
Drug Name
DEXTROAMPHETAMINE SULFATE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2015-11-23
Active Ingredient
DEXTROAMPHETAMINE SULFATE
Application Number
203548
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2015-11-23
Regulatory Status
RX
Drug Name
DEXTROAMPHETAMINE SULFATE
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2015-11-23
Active Ingredient
DEXTROAMPHETAMINE SULFATE
Application Number
203548
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2015-11-23
Regulatory Status
RX
Drug Name
DIETHYLPROPION HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2010-12-22
Active Ingredient
DIETHYLPROPION HYDROCHLORIDE
Application Number
201212
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2010-12-22
Regulatory Status
RX
Drug Name
HOMATROPINE METHYLBROMIDE AND HYDROCODONE BITARTRATE
Product Number
1
Dosage Form
-
Strength
1.5MG;5MG
Approval Date
2017-08-07
Active Ingredient
HOMATROPINE METHYLBROMIDE; HYDROCODONE BITARTRATE
Application Number
207176
Product Number
1
Dosage Form
-
Strength
1.5MG;5MG
Approval Date
2017-08-07
Regulatory Status
RX
Drug Name
INDOMETHACIN
Product Number
1
Dosage Form
-
Strength
75MG
Approval Date
2009-03-06
Active Ingredient
INDOMETHACIN
Application Number
79175
Product Number
1
Dosage Form
-
Strength
75MG
Approval Date
2009-03-06
Regulatory Status
RX
Drug Name
LOMAIRA
Product Number
1
Dosage Form
-
Strength
8MG
Approval Date
2016-09-12
Active Ingredient
PHENTERMINE HYDROCHLORIDE
Application Number
203495
Product Number
1
Dosage Form
-
Strength
8MG
Approval Date
2016-09-12
Regulatory Status
RX
Drug Name
OXYCODONE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2009-08-31
Active Ingredient
OXYCODONE HYDROCHLORIDE
Application Number
91393
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2009-08-31
Regulatory Status
RX
Drug Name
OXYCODONE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2009-08-31
Active Ingredient
OXYCODONE HYDROCHLORIDE
Application Number
91393
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2009-08-31
Regulatory Status
RX
Drug Name
OXYCODONE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
15MG
Approval Date
2009-08-31
Active Ingredient
OXYCODONE HYDROCHLORIDE
Application Number
91393
Product Number
3
Dosage Form
-
Strength
15MG
Approval Date
2009-08-31
Regulatory Status
RX
Drug Name
OXYCODONE HYDROCHLORIDE
Product Number
4
Dosage Form
-
Strength
20MG
Approval Date
2009-08-31
Active Ingredient
OXYCODONE HYDROCHLORIDE
Application Number
91393
Product Number
4
Dosage Form
-
Strength
20MG
Approval Date
2009-08-31
Regulatory Status
RX
Drug Name
OXYCODONE HYDROCHLORIDE
Product Number
5
Dosage Form
-
Strength
30MG
Approval Date
2009-08-31
Active Ingredient
OXYCODONE HYDROCHLORIDE
Application Number
91393
Product Number
5
Dosage Form
-
Strength
30MG
Approval Date
2009-08-31
Regulatory Status
RX
Drug Name
OXYCODONE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2015-08-17
Active Ingredient
OXYCODONE HYDROCHLORIDE
Application Number
202773
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2015-08-17
Regulatory Status
RX
Drug Name
OXYMORPHONE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2013-01-30
Active Ingredient
OXYMORPHONE HYDROCHLORIDE
Application Number
203601
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2013-01-30
Regulatory Status
RX
Drug Name
OXYMORPHONE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2013-01-30
Active Ingredient
OXYMORPHONE HYDROCHLORIDE
Application Number
203601
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2013-01-30
Regulatory Status
RX
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Drug Status Breakdown
16 total- OTC
- Discontinued
- RX
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
CHLORPHENIRAMINE MALEATE
Application Number
40829
Product Number
1
Active Ingredient
CHLORPHENIRAMINE MALEATE
Dosage Form
-
Strength
12MG
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