FDA Approved Drugs Database
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Drug Name:
AMPICILLIN AND SULBACTAM
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Application Number:
201406
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Product Number:
2
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Dosage Form:
INJECTABLE;INJECTION
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Strength:
EQ 2GM BASE/VIAL;EQ 1GM BASE/VIAL
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Product Type:
RX
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Active Ingredient:
AMPICILLIN SODIUM; SULBACTAM SODIUM
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Approval Date:
2015-12-07
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Legal Name:
-
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Drug Name:
SEMAGLUTIDE
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Application Number:
220314
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Product Number:
3
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Dosage Form:
INJECTION;SOLUTION
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Strength:
8MG/3ML
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Product Type:
-
Active Ingredient:
SEMAGLUTIDE
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Approval Date:
-
Legal Name:
-
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Drug Name:
SAPHNELO
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Application Number:
761451
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Product Number:
2
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Dosage Form:
INJECTION
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Strength:
120MG/0.8ML
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Product Type:
-
Active Ingredient:
ANIFROLUMAB-FNIA
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Approval Date:
-
Legal Name:
-
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Drug Name:
EVDI
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Application Number:
220837
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Product Number:
1
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Dosage Form:
SOLUTION;INTRAVENOUS
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Strength:
1MG/20ML (0.05MG/ML)
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Product Type:
RX
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Active Ingredient:
TRABECTEDIN
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Approval Date:
2026-05-01
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Legal Name:
-
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Drug Name:
DICLOFENAC SODIUM
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Application Number:
213040
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Product Number:
1
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Dosage Form:
SOLUTION;TOPICAL
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Strength:
2%
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Product Type:
RX
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Active Ingredient:
DICLOFENAC SODIUM
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Approval Date:
2023-02-03
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Legal Name:
-
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Drug Name:
OLEPTRO
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Application Number:
22411
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Product Number:
2
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Dosage Form:
TABLET, EXTENDED RELEASE;ORAL
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Strength:
300MG **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:
TRAZODONE HYDROCHLORIDE
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Approval Date:
2010-02-02
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Legal Name:
-
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Drug Name:
BACLOFEN
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Application Number:
217252
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Product Number:
1
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Dosage Form:
SUSPENSION;ORAL
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Strength:
25MG/5ML
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Product Type:
RX
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Active Ingredient:
BACLOFEN
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Approval Date:
2023-06-08
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Legal Name:
-
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Drug Name:
PRONESTYL-SR
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Application Number:
87361
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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:
1982-01-01
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Legal Name:
-
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Drug Name:
AUSTEDO XR
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Application Number:
216354
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Product Number:
8
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Dosage Form:
TABLET, EXTENDED RELEASE;ORAL
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Strength:
18MG
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Product Type:
RX
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Active Ingredient:
DEUTETRABENAZINE
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Approval Date:
2024-07-01
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Legal Name:
-
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Drug Name:
LOPERAMIDE HYDROCHLORIDE
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Application Number:
220372
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Product Number:
1
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Dosage Form:
CAPSULE;ORAL
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Strength:
2MG
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Product Type:
OTC
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Active Ingredient:
LOPERAMIDE HYDROCHLORIDE
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Approval Date:
2025-12-29
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Legal Name:
-
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