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Search results for "PART 172 -- FOOD ADDITIVES PERMITTED FOR DIRECT ADDITION TO FOOD FOR HUMAN CONSUMPTION" in comments (approximate match)
Status:
Possibly Marketed Outside US
Source:
M020
(2015)
Source URL:
First approved in 2015
Source:
M020
Source URL:
Class:
STRUCTURALLY DIVERSE
Status:
Possibly Marketed Outside US
Source:
21 CFR 352
(2013)
Source URL:
First approved in 2009
Source:
21 CFR 352
Source URL:
Class:
STRUCTURALLY DIVERSE
Status:
Possibly Marketed Outside US
Source:
21 CFR 348
(2009)
Source URL:
First approved in 2009
Source:
21 CFR 348
Source URL:
Class:
STRUCTURALLY DIVERSE
Status:
Possibly Marketed Outside US
Source:
Celladix Sebum Rebalancing Rx 131 Ampoule by 2359 US INC
(2023)
Source URL:
First approved in 2009
Source:
21 CFR 352
Source URL:
Class:
STRUCTURALLY DIVERSE
Status:
First approved in 2000
Source:
21 CFR 334
Source URL:
Class:
STRUCTURALLY DIVERSE
Status:
Possibly Marketed Outside US
Source:
21 CFR 348
(1995)
Source URL:
First approved in 1995
Source:
21 CFR 348
Source URL:
Class:
STRUCTURALLY DIVERSE
Status:
US Approved Rx
(1973)
Source:
NDA016931
(1973)
Source URL:
First approved in 1957
Class (Stereo):
CHEMICAL (ABSOLUTE)
Conditions:
L-arginine is a nonessential amino acid that may play an important role in the treatment of cardiovascular disease due to its antiatherogenic, anti-ischemic, antiplatelet, and antithrombotic properties. It has been promoted as a growth stimulant and as a treatment for erectile dysfunction in men. L-arginine is a nonessential amino acid that may play an important role in the treatment of heart disease due to its block arterial plaque buildup, blood clots, platelet clumping, and to increase blood flow through the coronary artery. L-arginine is commonly sold as a health supplement claiming to improve vascular health and treat erectile dysfunction in men. L-arginine, which is promoted as a human growth stimulant, has also been used in bodybuilding. In the 1800s, it was first isolated from animal horn.
Status:
US Approved Rx
(2023)
Source:
ANDA216435
(2023)
Source URL:
First approved in 1953
Source:
CALCIUM DISODIUM VERSENATE by BAUSCH
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Edetic acid (EDTA) is a chelating agent. The U.S. Food and Drug Administration (FDA) approved edetic acid chelation therapy as a treatment for lead and heavy metal poisoning. Edetic acid in form of disodium salt was withdrawn from the market due to death resulting from hypocalcemia during chelation.
Status:
US Approved Rx
(2023)
Source:
ANDA216435
(2023)
Source URL:
First approved in 1953
Source:
CALCIUM DISODIUM VERSENATE by BAUSCH
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Edetic acid (EDTA) is a chelating agent. The U.S. Food and Drug Administration (FDA) approved edetic acid chelation therapy as a treatment for lead and heavy metal poisoning. Edetic acid in form of disodium salt was withdrawn from the market due to death resulting from hypocalcemia during chelation.
Status:
US Approved Rx
(2023)
Source:
ANDA216435
(2023)
Source URL:
First approved in 1953
Source:
CALCIUM DISODIUM VERSENATE by BAUSCH
Source URL:
Class (Stereo):
CHEMICAL (ACHIRAL)
Conditions:
Edetic acid (EDTA) is a chelating agent. The U.S. Food and Drug Administration (FDA) approved edetic acid chelation therapy as a treatment for lead and heavy metal poisoning. Edetic acid in form of disodium salt was withdrawn from the market due to death resulting from hypocalcemia during chelation.
