FDA Approved Drugs Database
-
Drug Name:
OTIPRIO
-
Application Number:
207986
-
Product Number:
1
-
Dosage Form:
INJECTABLE, SUSPENSION;OTIC
-
Strength:
6% (60MG/ML)
-
Product Type:
DISCN
-
Active Ingredient:
CIPROFLOXACIN
-
Approval Date:
2015-12-10
-
Legal Name:
-
-
Drug Name:
BAFIERTAM
-
Application Number:
210296
-
Product Number:
1
-
Dosage Form:
CAPSULE, DELAYED RELEASE;ORAL
-
Strength:
95MG
-
Product Type:
RX
-
Active Ingredient:
MONOMETHYL FUMARATE
-
Approval Date:
2020-04-28
-
Legal Name:
-
-
Drug Name:
AURLUMYN
-
Application Number:
217933
-
Product Number:
1
-
Dosage Form:
SOLUTION;INTRAVENOUS
-
Strength:
100MCG/ML (100MCG/ML)
-
Product Type:
RX
-
Active Ingredient:
ILOPROST
-
Approval Date:
2024-02-13
-
Legal Name:
-
-
Drug Name:
CARBON DIOXIDE, USP
-
Application Number:
206025
-
Product Number:
1
-
Dosage Form:
GAS;INHALATION
-
Strength:
N/A
-
Product Type:
-
Active Ingredient:
CARBON DIOXIDE
-
Approval Date:
-
Legal Name:
-
-
Drug Name:
VOYDEYA
-
Application Number:
218037
-
Product Number:
2
-
Dosage Form:
TABLET;ORAL
-
Strength:
100MG
-
Product Type:
RX
-
Active Ingredient:
DANICOPAN
-
Approval Date:
2024-03-29
-
Legal Name:
-
-
Drug Name:
VALCYTE
-
Application Number:
22257
-
Product Number:
1
-
Dosage Form:
FOR SOLUTION;ORAL
-
Strength:
50MG/ML
-
Product Type:
RX
-
Active Ingredient:
VALGANCICLOVIR HYDROCHLORIDE
-
Approval Date:
2009-08-28
-
Legal Name:
-
-
Drug Name:
NOREPINEPHRINE BITARTRATE IN 5% DEXTROSE
-
Application Number:
220483
-
Product Number:
1
-
Dosage Form:
SOLUTION;INTRAVENOUS
-
Strength:
EQ 16MG BASE/250ML (EQ 64MCG BASE/ML)
-
Product Type:
RX
-
Active Ingredient:
NOREPINEPHRINE BITARTRATE
-
Approval Date:
2026-03-26
-
Legal Name:
-
-
Drug Name:
MECLIZINE HYDROCHLORIDE
-
Application Number:
88257
-
Product Number:
1
-
Dosage Form:
TABLET;ORAL
-
Strength:
25MG
-
Product Type:
DISCN
-
Active Ingredient:
MECLIZINE HYDROCHLORIDE
-
Approval Date:
1983-06-13
-
Legal Name:
-
Create a New Buying Request
Fields marked with * are mandatory.