KVK-TECH, INC. RX
FDA Approved Drugs
KVK-TECH, INC. RX
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 19
- Latest Approval Date Apr 03, 2015
- Data Source FDA
- First Approval Date Jul 31, 2006
Company Overview
Company
KVK-TECH, INC. RX
Country
U.S.A
Website
Social Profiles
Company Snapshot
KVK-TECH, INC. RX
KVK-TECH, Inc. 110 Terry Drive, Suite 200 Newtown, PA 18940 United States of America
U.S.A
kvktech.com/ Sales: sales@kvktech.com, General Information: contact@kvktech.com View on MapFDA Approved Drug Records ( 19 records )
Drug Name
BENZPHETAMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
2010-07-20
Active Ingredient
BENZPHETAMINE HYDROCHLORIDE
Application Number
90968
Product Number
1
Dosage Form
-
Strength
50MG
Approval Date
2010-07-20
Regulatory Status
RX
Drug Name
BETAXOLOL HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2008-06-27
Active Ingredient
BETAXOLOL HYDROCHLORIDE
Application Number
78962
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2008-06-27
Regulatory Status
RX
Drug Name
BETAXOLOL HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
20MG
Approval Date
2008-06-27
Active Ingredient
BETAXOLOL HYDROCHLORIDE
Application Number
78962
Product Number
2
Dosage Form
-
Strength
20MG
Approval Date
2008-06-27
Regulatory Status
RX
Drug Name
CYCLOBENZAPRINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2011-02-28
Active Ingredient
CYCLOBENZAPRINE HYDROCHLORIDE
Application Number
78048
Product Number
1
Dosage Form
-
Strength
5MG
Approval Date
2011-02-28
Regulatory Status
RX
Drug Name
CYCLOBENZAPRINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2011-02-28
Active Ingredient
CYCLOBENZAPRINE HYDROCHLORIDE
Application Number
78048
Product Number
2
Dosage Form
-
Strength
10MG
Approval Date
2011-02-28
Regulatory Status
RX
Drug Name
HYDROXYZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2007-03-20
Active Ingredient
HYDROXYZINE HYDROCHLORIDE
Application Number
40786
Product Number
1
Dosage Form
-
Strength
10MG
Approval Date
2007-03-20
Regulatory Status
RX
Drug Name
HYDROXYZINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
2007-03-20
Active Ingredient
HYDROXYZINE HYDROCHLORIDE
Application Number
40786
Product Number
2
Dosage Form
-
Strength
25MG
Approval Date
2007-03-20
Regulatory Status
RX
Drug Name
HYDROXYZINE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
2007-03-20
Active Ingredient
HYDROXYZINE HYDROCHLORIDE
Application Number
40786
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
2007-03-20
Regulatory Status
RX
Drug Name
KALEXATE
Product Number
1
Dosage Form
-
Strength
454GM/BOT
Approval Date
2009-03-30
Active Ingredient
SODIUM POLYSTYRENE SULFONATE
Application Number
40905
Product Number
1
Dosage Form
-
Strength
454GM/BOT
Approval Date
2009-03-30
Regulatory Status
RX
Drug Name
KALEXATE
Product Number
2
Dosage Form
-
Strength
15GM/BOT
Approval Date
2015-04-03
Active Ingredient
SODIUM POLYSTYRENE SULFONATE
Application Number
40905
Product Number
2
Dosage Form
-
Strength
15GM/BOT
Approval Date
2015-04-03
Regulatory Status
RX
Drug Name
PHENDIMETRAZINE TARTRATE
Product Number
1
Dosage Form
-
Strength
35MG
Approval Date
2010-08-31
Active Ingredient
PHENDIMETRAZINE TARTRATE
Application Number
91042
Product Number
1
Dosage Form
-
Strength
35MG
Approval Date
2010-08-31
Regulatory Status
RX
Drug Name
PHENTERMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
2008-03-21
Active Ingredient
PHENTERMINE HYDROCHLORIDE
Application Number
40875
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
2008-03-21
Regulatory Status
RX
Drug Name
PHENTERMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
37.5MG
Approval Date
2008-03-31
Active Ingredient
PHENTERMINE HYDROCHLORIDE
Application Number
40876
Product Number
1
Dosage Form
-
Strength
37.5MG
Approval Date
2008-03-31
Regulatory Status
RX
Drug Name
PHENTERMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
2008-03-31
Active Ingredient
PHENTERMINE HYDROCHLORIDE
Application Number
40886
Product Number
1
Dosage Form
-
Strength
30MG
Approval Date
2008-03-31
Regulatory Status
RX
Drug Name
PHENTERMINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
15MG
Approval Date
2008-03-31
Active Ingredient
PHENTERMINE HYDROCHLORIDE
Application Number
40886
Product Number
2
Dosage Form
-
Strength
15MG
Approval Date
2008-03-31
Regulatory Status
RX
Drug Name
PHENTERMINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
37.5MG
Approval Date
2008-04-24
Active Ingredient
PHENTERMINE HYDROCHLORIDE
Application Number
40887
Product Number
1
Dosage Form
-
Strength
37.5MG
Approval Date
2008-04-24
Regulatory Status
RX
Drug Name
PROMETHAZINE HYDROCHLORIDE
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2006-07-31
Active Ingredient
PROMETHAZINE HYDROCHLORIDE
Application Number
40712
Product Number
1
Dosage Form
-
Strength
25MG
Approval Date
2006-07-31
Regulatory Status
RX
Drug Name
PROMETHAZINE HYDROCHLORIDE
Product Number
2
Dosage Form
-
Strength
12.5MG
Approval Date
2007-05-04
Active Ingredient
PROMETHAZINE HYDROCHLORIDE
Application Number
40712
Product Number
2
Dosage Form
-
Strength
12.5MG
Approval Date
2007-05-04
Regulatory Status
RX
Drug Name
PROMETHAZINE HYDROCHLORIDE
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
2006-07-31
Active Ingredient
PROMETHAZINE HYDROCHLORIDE
Application Number
40712
Product Number
3
Dosage Form
-
Strength
50MG
Approval Date
2006-07-31
Regulatory Status
RX
Related Databases
-
FDA Inspections
0 View
-
EDQM CEP
0 View
-
KDMF
0 View
-
Japan DMF
0 View
-
Eudra GMP
0 View
-
NDC Database
0 View
-
FDA Approved Drugs Database
20 View
-
Drug Prices in Switzerland
0 View
Drug Status Breakdown
19 total- 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
BENZPHETAMINE HYDROCHLORIDE
Application Number
90968
Product Number
1
Active Ingredient
BENZPHETAMINE HYDROCHLORIDE
Dosage Form
-
Strength
50MG
FDA Approved Drug Data
Approved drug product information
Regular Updates
Data maintained from official sources
Structured Database
Searchable pharmaceutical data
Reliable Data
Organized FDA drug records
Create a New Buying Request
Fields marked with * are mandatory.