FDA Approved Drugs Database
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Drug Name:
HELIUM, USP
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Application Number:
206026
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Product Number:
1
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Dosage Form:
GAS;INHALATION
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Strength:
N/A
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Product Type:
-
Active Ingredient:
HELIUM
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Approval Date:
-
Legal Name:
-
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Drug Name:
ALTAFLUOR BENOX
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Application Number:
208582
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Product Number:
1
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Dosage Form:
SOLUTION/DROPS;OPHTHALMIC
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Strength:
0.4%;0.25%
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Product Type:
RX
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Active Ingredient:
BENOXINATE HYDROCHLORIDE; FLUORESCEIN SODIUM
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Approval Date:
2017-12-14
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Legal Name:
-
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Drug Name:
DESVENLAFAXINE
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Application Number:
204009
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Product Number:
2
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Dosage Form:
TABLET, EXTENDED RELEASE;ORAL
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Strength:
100MG
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Product Type:
-
Active Ingredient:
DESVENLAFAXINE
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Approval Date:
-
Legal Name:
-
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Drug Name:
EMPAGLIFLOZIN AND METFORMIN HYDROCHLORIDE
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Application Number:
220511
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Product Number:
4
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Dosage Form:
TABLET, EXTENDED RELEASE
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Strength:
25MG/1000MG
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Product Type:
-
Active Ingredient:
EMPAGLIFLOZIN, METFORMIN HYDROCHLORIDE
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Approval Date:
-
Legal Name:
-
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Drug Name:
TIMOLOL MALEATE
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Application Number:
204912
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Product Number:
1
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Dosage Form:
SOLUTION;OPHTHALMIC
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Strength:
0.5%
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Product Type:
-
Active Ingredient:
TIMOLOL MALEATE
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Approval Date:
-
Legal Name:
-
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Drug Name:
LAROTRECTINIB
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Application Number:
220639
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Product Number:
1
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Dosage Form:
CAPSULE
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Strength:
100MG
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Product Type:
-
Active Ingredient:
LAROTRECTINIB
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Approval Date:
-
Legal Name:
-
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Drug Name:
RIFAXIMIN
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Application Number:
220451
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Product Number:
2
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Dosage Form:
TABLET
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Strength:
200MG
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Product Type:
-
Active Ingredient:
RIFAXIMIN
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Approval Date:
-
Legal Name:
-
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Drug Name:
ISOSORBIDE MONONITRATE
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Application Number:
75041
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Product Number:
1
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Dosage Form:
TABLET, EXTENDED RELEASE;ORAL
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Strength:
60MG
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Product Type:
DISCN
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Active Ingredient:
ISOSORBIDE MONONITRATE
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Approval Date:
1998-09-22
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Legal Name:
-
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Drug Name:
ALBALON
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Application Number:
80248
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Product Number:
1
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Dosage Form:
SOLUTION/DROPS;OPHTHALMIC
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Strength:
0.1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
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Product Type:
DISCN
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Active Ingredient:
NAPHAZOLINE HYDROCHLORIDE
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Approval Date:
1982-01-01
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Legal Name:
-
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Drug Name:
RALOXIFENE HYDROCHLORIDE
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Application Number:
208206
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Product Number:
1
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Dosage Form:
TABLET;ORAL
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Strength:
60MG
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Product Type:
RX
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Active Ingredient:
RALOXIFENE HYDROCHLORIDE
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Approval Date:
2016-04-08
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Legal Name:
-
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