FDA Approved Drugs Database
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Drug Name:
TISSUEBLUE
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Application Number:
209569
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Product Number:
1
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Dosage Form:
SOLUTION;OPHTHALMIC
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Strength:
0.025%
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Product Type:
RX
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Active Ingredient:
BRILLIANT BLUE G
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Approval Date:
2019-12-20
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Legal Name:
-
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Drug Name:
TOLAK
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Application Number:
22259
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Product Number:
1
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Dosage Form:
CREAM;TOPICAL
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Strength:
4%
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Product Type:
RX
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Active Ingredient:
FLUOROURACIL
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Approval Date:
2015-09-18
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Legal Name:
-
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Drug Name:
PUR-WASH
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Application Number:
22305
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Product Number:
1
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Dosage Form:
SOLUTION;OPHTHALMIC
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Strength:
98.3%
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Product Type:
OTC
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Active Ingredient:
PURIFIED WATER
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Approval Date:
2011-09-01
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Legal Name:
-
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Drug Name:
OXYGEN, USP
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Application Number:
205986
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Product Number:
1
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Dosage Form:
GAS;INHALATION
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Strength:
N/A
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Product Type:
-
Active Ingredient:
OXYGEN
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Approval Date:
-
Legal Name:
-
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Drug Name:
PAROEX
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Application Number:
76434
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Product Number:
1
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Dosage Form:
SOLUTION;DENTAL
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Strength:
0.12%
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Product Type:
DISCN
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Active Ingredient:
CHLORHEXIDINE GLUCONATE
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Approval Date:
2005-11-29
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Legal Name:
-
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Drug Name:
GONAL-F
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Application Number:
21765
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Product Number:
3
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Dosage Form:
INJECTABLE;SUBCUTANEOUS
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Strength:
150 IU/VIAL
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Product Type:
-
Active Ingredient:
FOLLITROPIN ALFA/BETA
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Approval Date:
-
Legal Name:
-
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Drug Name:
NASALCROM
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Application Number:
20463
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Product Number:
1
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Dosage Form:
SPRAY, METERED;NASAL
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Strength:
5.2MG/SPRAY **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:
CROMOLYN SODIUM
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Approval Date:
1997-01-03
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Legal Name:
-
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Drug Name:
NEBIVOLOL HYDROCHLORIDE
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Application Number:
212917
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Product Number:
4
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Dosage Form:
TABLET;ORAL
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Strength:
EQ 20MG BASE
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Product Type:
RX
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Active Ingredient:
NEBIVOLOL HYDROCHLORIDE
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Approval Date:
2021-12-17
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Legal Name:
-
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Drug Name:
METHYLENE BLUE
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Application Number:
219550
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Product Number:
1
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Dosage Form:
SOLUTION;INTRAVENOUS
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Strength:
50MG/10ML (5MG/ML)
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Product Type:
RX
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Active Ingredient:
METHYLENE BLUE
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Approval Date:
2025-12-23
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Legal Name:
-
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Drug Name:
ETHACRYNATE SODIUM
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Application Number:
208663
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Product Number:
1
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Dosage Form:
INJECTABLE;INJECTION
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Strength:
EQ 50MG BASE/VIAL
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Product Type:
RX
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Active Ingredient:
ETHACRYNATE SODIUM
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Approval Date:
2020-06-09
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Legal Name:
-
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