FDA Approved Drugs Database
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Drug Name:
NUEDEXTA
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Application Number:
21879
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Product Number:
1
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Dosage Form:
CAPSULE;ORAL
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Strength:
20MG;10MG
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Product Type:
RX
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Active Ingredient:
DEXTROMETHORPHAN HYDROBROMIDE; QUINIDINE SULFATE
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Approval Date:
2010-10-29
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Legal Name:
-
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Drug Name:
AMIODARONE HYDROCHLORIDE
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Application Number:
76394
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Product Number:
1
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Dosage Form:
INJECTABLE;INJECTION
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Strength:
50MG/ML
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Product Type:
DISCN
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Active Ingredient:
AMIODARONE HYDROCHLORIDE
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Approval Date:
2003-04-25
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Legal Name:
-
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Drug Name:
DIDRONEL
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Application Number:
19545
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Product Number:
1
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Dosage Form:
INJECTABLE;INJECTION
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Strength:
50MG/ML
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Product Type:
DISCN
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Active Ingredient:
ETIDRONATE DISODIUM
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Approval Date:
1987-04-20
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Legal Name:
-
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Drug Name:
ZELBORAF
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Application Number:
202429
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Product Number:
1
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Dosage Form:
TABLET;ORAL
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Strength:
240MG
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Product Type:
RX
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Active Ingredient:
VEMURAFENIB
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Approval Date:
2011-08-17
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Legal Name:
-
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Drug Name:
TYENNE
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Application Number:
761449
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Product Number:
4
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Dosage Form:
INJECTABLE;SUBCUTANEOUS
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Strength:
162MG/0.9ML
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Product Type:
-
Active Ingredient:
TOCILIZUMAB-AAZG
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Approval Date:
-
Legal Name:
-
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Drug Name:
NAFCILLIN SODIUM
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Application Number:
206761
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Product Number:
1
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Dosage Form:
INJECTABLE;INJECTION
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Strength:
EQ 10GM BASE/VIAL
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Product Type:
DISCN
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Active Ingredient:
NAFCILLIN SODIUM
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Approval Date:
2020-06-02
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Legal Name:
-
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Drug Name:
LACOSAMIDE
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Application Number:
220268
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Product Number:
1
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Dosage Form:
SOLUTION;INTRAVENOUS
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Strength:
200MG/20ML (10MG/ML)
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Product Type:
RX
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Active Ingredient:
LACOSAMIDE
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Approval Date:
2026-01-21
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Legal Name:
-
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Drug Name:
CRYSVITA
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Application Number:
761068
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Product Number:
1
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Dosage Form:
INJECTABLE;INJECTION
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Strength:
10MG/ML
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Product Type:
-
Active Ingredient:
BUROSUMAB-TWZA
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Approval Date:
-
Legal Name:
-
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Drug Name:
LEVOTHYROXINE SODIUM
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Application Number:
76752
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Product Number:
11
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Dosage Form:
TABLET;ORAL
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Strength:
0.3MG
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Product Type:
DISCN
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Active Ingredient:
LEVOTHYROXINE SODIUM
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Approval Date:
2005-06-16
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Legal Name:
-
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Drug Name:
SIMTRIYO
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Application Number:
218145
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Product Number:
1
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Dosage Form:
CAPSULE, EXTENDED RELEASE
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Strength:
280MG
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Product Type:
-
Active Ingredient:
CENTANAFADINE HYDROCHLORIDE
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Approval Date:
-
Legal Name:
-
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