FDA Approved Drugs Database
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Drug Name:
FLUOCINOLONE ACETONIDE
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Application Number:
88045
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Product Number:
1
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Dosage Form:
CREAM;TOPICAL
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Strength:
0.025%
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Product Type:
DISCN
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Active Ingredient:
FLUOCINOLONE ACETONIDE
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Approval Date:
1982-12-16
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Legal Name:
-
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Drug Name:
NALOXONE HYDROCHLORIDE
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Application Number:
219942
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Product Number:
2
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Dosage Form:
INJECTABLE;INJECTION
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Strength:
1MG/ML
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Product Type:
-
Active Ingredient:
NALOXONE HYDROCHLORIDE
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Approval Date:
-
Legal Name:
-
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Drug Name:
POTASSIUM CHLORIDE
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Application Number:
213062
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Product Number:
2
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Dosage Form:
SOLUTION;ORAL
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Strength:
40MEQ/15ML
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Product Type:
RX
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Active Ingredient:
POTASSIUM CHLORIDE
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Approval Date:
2022-06-06
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Legal Name:
-
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Drug Name:
BENTYL
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Application Number:
7961
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Product Number:
2
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Dosage Form:
SYRUP;ORAL
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Strength:
10MG/5ML **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**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:
DICYCLOMINE HYDROCHLORIDE
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Approval Date:
1984-10-15
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Legal Name:
-
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Drug Name:
P.A.S. SODIUM
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Application Number:
80947
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Product Number:
1
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Dosage Form:
POWDER;ORAL
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Strength:
4GM/PACKET
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Product Type:
DISCN
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Active Ingredient:
AMINOSALICYLATE SODIUM
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Approval Date:
1982-01-01
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Legal Name:
-
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Drug Name:
MEZOFY
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Application Number:
211448
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Product Number:
3
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Dosage Form:
FILM;ORAL
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Strength:
15MG
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Product Type:
DISCN
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Active Ingredient:
ARIPIPRAZOLE
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Approval Date:
2025-04-15
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Legal Name:
-
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Drug Name:
TRIENTINE HYDROCHLORIDE
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Application Number:
209945
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Product Number:
1
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Dosage Form:
CAPSULE;ORAL
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Strength:
250MG
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Product Type:
RX
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Active Ingredient:
TRIENTINE HYDROCHLORIDE
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Approval Date:
2021-08-13
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Legal Name:
-
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Drug Name:
RIVAROXABAN
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Application Number:
220874
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Product Number:
4
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Dosage Form:
TABLET;ORAL
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Strength:
20MG
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Product Type:
RX
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Active Ingredient:
RIVAROXABAN
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Approval Date:
2026-07-01
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Legal Name:
-
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Drug Name:
MEMANTINE HYDROCHLORIDE
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Application Number:
210319
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Product Number:
1
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Dosage Form:
SOLUTION;ORAL
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Strength:
2MG/ML
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Product Type:
RX
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Active Ingredient:
MEMANTINE HYDROCHLORIDE
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Approval Date:
2020-08-31
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Legal Name:
-
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Drug Name:
ZAFIRLUKAST
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Application Number:
204928
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Product Number:
2
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Dosage Form:
TABLET;ORAL
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Strength:
20MG
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Product Type:
RX
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Active Ingredient:
ZAFIRLUKAST
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Approval Date:
2022-08-25
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Legal Name:
-
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