FDA Approved Drugs Database
-
Drug Name:
NITROFURANTOIN (MONOHYDRATE/MACROCRYSTALS)
-
Application Number:
220269
-
Product Number:
1
-
Dosage Form:
CAPSULE;ORAL
-
Strength:
75MG;25MG
-
Product Type:
RX
-
Active Ingredient:
NITROFURANTOIN; NITROFURANTOIN, MACROCRYSTALLINE
-
Approval Date:
2026-04-07
-
Legal Name:
-
-
Drug Name:
RIVIVE
-
Application Number:
217722
-
Product Number:
1
-
Dosage Form:
SPRAY, METERED;NASAL
-
Strength:
3MG/SPRAY
-
Product Type:
OTC
-
Active Ingredient:
NALOXONE HYDROCHLORIDE
-
Approval Date:
2023-07-28
-
Legal Name:
-
-
Drug Name:
FLECAINIDE ACETATE
-
Application Number:
218093
-
Product Number:
3
-
Dosage Form:
TABLET;ORAL
-
Strength:
150MG
-
Product Type:
RX
-
Active Ingredient:
FLECAINIDE ACETATE
-
Approval Date:
2026-04-22
-
Legal Name:
-
-
Drug Name:
CUVRIOR
-
Application Number:
215760
-
Product Number:
1
-
Dosage Form:
TABLET;ORAL
-
Strength:
300MG
-
Product Type:
RX
-
Active Ingredient:
TRIENTINE TETRAHYDROCHLORIDE
-
Approval Date:
2022-04-28
-
Legal Name:
-
-
Drug Name:
PIPERACILLIN AND TAZOBACTAM
-
Application Number:
217243
-
Product Number:
1
-
Dosage Form:
INJECTABLE;INJECTION
-
Strength:
EQ 36GM BASE/VIAL;EQ 4.5GM BASE/VIAL
-
Product Type:
RX
-
Active Ingredient:
PIPERACILLIN SODIUM; TAZOBACTAM SODIUM
-
Approval Date:
2023-04-14
-
Legal Name:
-
-
Drug Name:
CARBOPROST TROMETHAMINE
-
Application Number:
216824
-
Product Number:
1
-
Dosage Form:
INJECTABLE;INJECTION
-
Strength:
EQ 0.25MG BASE/ML
-
Product Type:
RX
-
Active Ingredient:
CARBOPROST TROMETHAMINE
-
Approval Date:
2023-05-19
-
Legal Name:
-
-
Drug Name:
CAPECITABINE
-
Application Number:
217237
-
Product Number:
2
-
Dosage Form:
TABLET;ORAL
-
Strength:
500MG
-
Product Type:
RX
-
Active Ingredient:
CAPECITABINE
-
Approval Date:
2023-10-23
-
Legal Name:
-
-
Drug Name:
CYKLX
-
Application Number:
218643
-
Product Number:
1
-
Dosage Form:
SOLUTION/DROPS;OPHTHALMIC
-
Strength:
EQ 8% BASE
-
Product Type:
DISCN
-
Active Ingredient:
ARTICAINE HYDROCHLORIDE
-
Approval Date:
2025-08-15
-
Legal Name:
-
-
Drug Name:
NEPHROSCAN
-
Application Number:
214993
-
Product Number:
1
-
Dosage Form:
POWDER;INTRAVENOUS
-
Strength:
N/A
-
Product Type:
RX
-
Active Ingredient:
TECHNETIUM TC-99M SUCCIMER
-
Approval Date:
2022-02-18
-
Legal Name:
-
-
Drug Name:
ELEPSIA XR
-
Application Number:
204417
-
Product Number:
2
-
Dosage Form:
TABLET, EXTENDED RELEASE;ORAL
-
Strength:
1.5GM
-
Product Type:
DISCN
-
Active Ingredient:
LEVETIRACETAM
-
Approval Date:
2018-12-20
-
Legal Name:
-
Create a New Buying Request
Fields marked with * are mandatory.