FDA Approved Drugs Database
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Drug Name:
METOPROLOL SUCCINATE
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Application Number:
207206
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Product Number:
4
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Dosage Form:
TABLET, EXTENDED RELEASE;ORAL
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Strength:
EQ 200MG TARTRATE
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Product Type:
RX
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Active Ingredient:
METOPROLOL SUCCINATE
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Approval Date:
2018-12-19
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Legal Name:
-
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Drug Name:
PHENYTOIN SODIUM
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Application Number:
89900
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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:
PHENYTOIN SODIUM
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Approval Date:
1990-03-30
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Legal Name:
-
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Drug Name:
ROCURONIUM BROMIDE
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Application Number:
204679
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Product Number:
2
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Dosage Form:
INJECTABLE;INJECTION
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Strength:
100MG/10ML (10MG/ML)
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Product Type:
RX
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Active Ingredient:
ROCURONIUM BROMIDE
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Approval Date:
2017-02-28
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Legal Name:
-
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Drug Name:
TOFACITINIB CITRATE
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Application Number:
215552
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Product Number:
2
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Dosage Form:
TABLET;ORAL
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Strength:
EQ 10MG BASE
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Product Type:
RX
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Active Ingredient:
TOFACITINIB CITRATE
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Approval Date:
2026-06-09
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Legal Name:
-
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Drug Name:
MICAFUNGIN SODIUM
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Application Number:
211713
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Product Number:
2
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Dosage Form:
INJECTABLE;INTRAVENOUS
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Strength:
EQ 100MG BASE/VIAL
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Product Type:
RX
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Active Ingredient:
MICAFUNGIN SODIUM
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Approval Date:
2021-06-02
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Legal Name:
-
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Drug Name:
ENTECAVIR
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Application Number:
208195
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Product Number:
2
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Dosage Form:
TABLET;ORAL
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Strength:
1MG
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Product Type:
RX
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Active Ingredient:
ENTECAVIR
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Approval Date:
2021-11-10
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Legal Name:
-
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Drug Name:
OLOPATADINE HYDROCHLORIDE
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Application Number:
204706
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Product Number:
1
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Dosage Form:
SOLUTION/DROPS;OPHTHALMIC
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Strength:
EQ 0.1% BASE
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Product Type:
DISCN
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Active Ingredient:
OLOPATADINE HYDROCHLORIDE
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Approval Date:
2015-12-07
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Legal Name:
-
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Drug Name:
MYCOPHENOLATE MOFETIL
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Application Number:
204077
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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:
MYCOPHENOLATE MOFETIL
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Approval Date:
2017-11-13
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Legal Name:
-
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