FDA Approved Drugs Database
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Drug Name:
REBIF
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Application Number:
103780
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Product Number:
2
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Dosage Form:
SYRINGE
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Strength:
44UG/0.5ML
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Product Type:
-
Active Ingredient:
INTERFERON BETA-1A
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Approval Date:
-
Legal Name:
-
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Drug Name:
VOYXACT
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Application Number:
761434
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Product Number:
1
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Dosage Form:
INJECTABLE;INJECTION
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Strength:
400MG/2ML(200MG/ML)
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Product Type:
-
Active Ingredient:
SIBEPRENLIMAB-SZSI
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Approval Date:
-
Legal Name:
-
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Drug Name:
TIMOLOL MALEATE
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Application Number:
74747
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Product Number:
1
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Dosage Form:
SOLUTION/DROPS;OPHTHALMIC
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Strength:
EQ 0.5% BASE
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Product Type:
RX
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Active Ingredient:
TIMOLOL MALEATE
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Approval Date:
1997-03-25
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Legal Name:
-
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Drug Name:
METHOCARBAMOL AND ASPIRIN
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Application Number:
89193
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Product Number:
1
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Dosage Form:
TABLET;ORAL
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Strength:
325MG;400MG
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Product Type:
DISCN
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Active Ingredient:
ASPIRIN; METHOCARBAMOL
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Approval Date:
1986-02-12
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Legal Name:
-
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Drug Name:
PROVOCHOLINE
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Application Number:
19193
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Product Number:
2
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Dosage Form:
FOR SOLUTION;INHALATION
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Strength:
1600MG/VIAL
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Product Type:
DISCN
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Active Ingredient:
METHACHOLINE CHLORIDE
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Approval Date:
2016-08-29
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Legal Name:
-
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Drug Name:
ABILIFY ASIMTUFII
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Application Number:
217006
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Product Number:
2
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Dosage Form:
SUSPENSION, EXTENDED RELEASE;INTRAMUSCULAR
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Strength:
960MG/3.2ML (300MG/ML)
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Product Type:
RX
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Active Ingredient:
ARIPIPRAZOLE
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Approval Date:
2023-04-27
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Legal Name:
-
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Drug Name:
LAMIVUDINE AND ZIDOVUDINE
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Application Number:
22018
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Product Number:
1
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Dosage Form:
TABLET;ORAL
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Strength:
150MG;300MG
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Product Type:
DISCN
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Active Ingredient:
LAMIVUDINE; ZIDOVUDINE
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Approval Date:
2017-03-17
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Legal Name:
-
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Drug Name:
PALIPERIDONE PALMITATE
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Application Number:
210397
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Product Number:
1
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Dosage Form:
SUSPENSION;EXTENDED RELEASE
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Strength:
-
Product Type:
-
Active Ingredient:
PALIPERIDONE PALMITATE
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Approval Date:
-
Legal Name:
-
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Drug Name:
ETOPOSIDE
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Application Number:
74813
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Product Number:
1
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Dosage Form:
INJECTABLE;INJECTION
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Strength:
20MG/ML
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Product Type:
DISCN
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Active Ingredient:
ETOPOSIDE
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Approval Date:
1997-07-09
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Legal Name:
-
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Drug Name:
ENTYVIO
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Application Number:
761359
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Product Number:
2
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Dosage Form:
INJECTABLE;SUBCUTANEOUS
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Strength:
108MG/0.68ML
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Product Type:
-
Active Ingredient:
VEDOLIZUMAB
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Approval Date:
-
Legal Name:
-
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