FDA Approved Drugs Database
-
Drug Name:
METHOCARBAMOL
-
Application Number:
203550
-
Product Number:
2
-
Dosage Form:
TABLET;ORAL
-
Strength:
750MG
-
Product Type:
RX
-
Active Ingredient:
METHOCARBAMOL
-
Approval Date:
2017-02-08
-
Legal Name:
-
-
Drug Name:
POTASSIUM CHLORIDE
-
Application Number:
214395
-
Product Number:
2
-
Dosage Form:
TABLET, EXTENDED RELEASE;ORAL
-
Strength:
20MEQ
-
Product Type:
RX
-
Active Ingredient:
POTASSIUM CHLORIDE
-
Approval Date:
2021-01-28
-
Legal Name:
-
-
Drug Name:
NUTRACORT
-
Application Number:
84698
-
Product Number:
1
-
Dosage Form:
GEL;TOPICAL
-
Strength:
1% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
-
Product Type:
DISCN
-
Active Ingredient:
HYDROCORTISONE
-
Approval Date:
1982-01-01
-
Legal Name:
-
-
Drug Name:
BIOSCRUB
-
Application Number:
19822
-
Product Number:
1
-
Dosage Form:
SPONGE;TOPICAL
-
Strength:
4%
-
Product Type:
OTC
-
Active Ingredient:
CHLORHEXIDINE GLUCONATE
-
Approval Date:
1989-03-31
-
Legal Name:
-
-
Drug Name:
TECHNETIUM TC99M MERTIATIDE KIT
-
Application Number:
206489
-
Product Number:
1
-
Dosage Form:
INJECTABLE;INJECTION
-
Strength:
N/A
-
Product Type:
RX
-
Active Ingredient:
TECHNETIUM TC-99M MERTIATIDE KIT
-
Approval Date:
2020-02-06
-
Legal Name:
-
-
Drug Name:
MOXIDECTIN
-
Application Number:
210867
-
Product Number:
1
-
Dosage Form:
TABLET;ORAL
-
Strength:
2MG
-
Product Type:
RX
-
Active Ingredient:
MOXIDECTIN
-
Approval Date:
2018-06-13
-
Legal Name:
-
-
Drug Name:
SUBSYS
-
Application Number:
202788
-
Product Number:
7
-
Dosage Form:
SPRAY;SUBLINGUAL
-
Strength:
1.6MG **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
-
Product Type:
DISCN
-
Active Ingredient:
FENTANYL
-
Approval Date:
2012-08-30
-
Legal Name:
-
-
Drug Name:
XENOVIEW
-
Application Number:
214375
-
Product Number:
1
-
Dosage Form:
GAS;INHALATION
-
Strength:
N/A
-
Product Type:
RX
-
Active Ingredient:
XENON XE-129 HYPERPOLARIZED
-
Approval Date:
2022-12-23
-
Legal Name:
-
-
Drug Name:
ROXYBOND
-
Application Number:
209777
-
Product Number:
4
-
Dosage Form:
TABLET;ORAL
-
Strength:
10MG
-
Product Type:
RX
-
Active Ingredient:
OXYCODONE HYDROCHLORIDE
-
Approval Date:
2024-09-05
-
Legal Name:
-
Create a New Buying Request
Fields marked with * are mandatory.