FDA Approved Drugs Database
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Drug Name:
ALBUTEROL SULFATE
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Application Number:
77569
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Product Number:
1
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Dosage Form:
SOLUTION;INHALATION
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Strength:
EQ 0.083% BASE
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Product Type:
DISCN
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Active Ingredient:
ALBUTEROL SULFATE
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Approval Date:
2006-04-04
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Legal Name:
-
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Drug Name:
K+10
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Application Number:
70999
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Product Number:
1
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Dosage Form:
TABLET, EXTENDED RELEASE;ORAL
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Strength:
10MEQ
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Product Type:
DISCN
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Active Ingredient:
POTASSIUM CHLORIDE
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Approval Date:
1987-10-22
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Legal Name:
-
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Drug Name:
HYDROCODONE BITARTRATE AND ACETAMINOPHEN
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Application Number:
89971
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Product Number:
1
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Dosage Form:
TABLET;ORAL
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Strength:
500MG;5MG
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Product Type:
DISCN
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Active Ingredient:
ACETAMINOPHEN; HYDROCODONE BITARTRATE
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Approval Date:
1988-12-02
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Legal Name:
-
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Drug Name:
NICOTINE POLACRILEX
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Application Number:
214354
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Product Number:
1
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Dosage Form:
GUM, CHEWING;BUCCAL
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Strength:
EQ 4MG BASE
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Product Type:
DISCN
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Active Ingredient:
NICOTINE POLACRILEX
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Approval Date:
2022-12-21
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Legal Name:
-
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Drug Name:
PROCAINAMIDE HYDROCHLORIDE
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Application Number:
89840
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Product Number:
1
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Dosage Form:
TABLET, EXTENDED RELEASE;ORAL
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Strength:
500MG
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Product Type:
DISCN
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Active Ingredient:
PROCAINAMIDE HYDROCHLORIDE
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Approval Date:
1989-03-06
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Legal Name:
-
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Drug Name:
TAZAROTENE
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Application Number:
211175
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Product Number:
1
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Dosage Form:
CREAM;TOPICAL
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Strength:
0.1%
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Product Type:
DISCN
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Active Ingredient:
TAZAROTENE
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Approval Date:
2019-01-28
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Legal Name:
-
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Drug Name:
PIPERACILLIN AND TAZOBACTAM
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Application Number:
203720
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Product Number:
1
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Dosage Form:
INJECTABLE;INJECTION
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Strength:
EQ 36GM BASE/VIAL;EQ 4.5GM BASE/VIAL
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Product Type:
RX
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Active Ingredient:
PIPERACILLIN SODIUM; TAZOBACTAM SODIUM
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Approval Date:
2018-05-11
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Legal Name:
-
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Drug Name:
FLUOXETINE HYDROCHLORIDE
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Application Number:
212191
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Product Number:
1
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Dosage Form:
TABLET;ORAL
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Strength:
EQ 60MG BASE
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Product Type:
DISCN
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Active Ingredient:
FLUOXETINE HYDROCHLORIDE
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Approval Date:
2019-07-05
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Legal Name:
-
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Drug Name:
PIXXOSCAN
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Application Number:
215957
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Product Number:
4
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Dosage Form:
SOLUTION;INTRAVENOUS
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Strength:
9.0708GM/15ML (604.72MG/ML)
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Product Type:
RX
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Active Ingredient:
GADOBUTROL
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Approval Date:
2026-06-29
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Legal Name:
-
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