FDA Approved Drugs Database
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Drug Name:
PROSTEP
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Application Number:
19983
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Product Number:
4
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Dosage Form:
FILM, EXTENDED RELEASE;TRANSDERMAL
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Strength:
22MG/24HR
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Product Type:
DISCN
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Active Ingredient:
NICOTINE
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Approval Date:
1998-12-23
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Legal Name:
-
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Drug Name:
CHLOROTRIANISENE
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Application Number:
84652
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Product Number:
1
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Dosage Form:
CAPSULE;ORAL
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Strength:
12MG
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Product Type:
DISCN
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Active Ingredient:
CHLOROTRIANISENE
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Approval Date:
1982-01-01
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Legal Name:
-
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Drug Name:
ACAMPROSATE CALCIUM
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Application Number:
200143
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Product Number:
1
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Dosage Form:
TABLET, DELAYED RELEASE;ORAL
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Strength:
333MG
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Product Type:
DISCN
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Active Ingredient:
ACAMPROSATE CALCIUM
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Approval Date:
2013-11-18
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Legal Name:
-
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Drug Name:
AMPICILLIN TRIHYDRATE
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Application Number:
61602
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Product Number:
2
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Dosage Form:
CAPSULE;ORAL
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Strength:
EQ 500MG BASE
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Product Type:
DISCN
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Active Ingredient:
AMPICILLIN/AMPICILLIN TRIHYDRATE
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Approval Date:
1982-01-01
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Legal Name:
-
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Drug Name:
BALANCED SALT
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Application Number:
91387
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Product Number:
1
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Dosage Form:
SOLUTION;IRRIGATION
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Strength:
0.48MG/ML;0.3MG/ML;0.75MG/ML;3.9MG/ML;6.4MG/ML;1.7MG/ML
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Product Type:
RX
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Active Ingredient:
CALCIUM CHLORIDE; MAGNESIUM CHLORIDE; POTASSIUM CHLORIDE; SODIUM ACETATE; SODIUM CHLORIDE; SODIUM CITRATE
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Approval Date:
2010-02-03
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Legal Name:
-
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Drug Name:
VYZULTA
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Application Number:
207795
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Product Number:
1
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Dosage Form:
SOLUTION/DROPS;OPHTHALMIC
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Strength:
0.024%
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Product Type:
RX
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Active Ingredient:
LATANOPROSTENE BUNOD
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Approval Date:
2017-11-02
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Legal Name:
-
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Drug Name:
EPINEPHRINE
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Application Number:
220626
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Product Number:
2
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Dosage Form:
SOLUTION;INTRAMUSCULAR, INTRAVENOUS, SUBCUTANEOUS
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Strength:
30MG/30ML (1MG/ML)
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Product Type:
RX
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Active Ingredient:
EPINEPHRINE
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Approval Date:
2026-03-30
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Legal Name:
-
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Drug Name:
RIBAVIRIN
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Application Number:
202546
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Product Number:
4
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Dosage Form:
TABLET;ORAL
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Strength:
600MG
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Product Type:
DISCN
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Active Ingredient:
RIBAVIRIN
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Approval Date:
2014-08-12
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Legal Name:
-
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