NDC 42023-243

EPHEDRINE SULFATE

Ephedrine Sulfate

EPHEDRINE SULFATE is a Intravenous Injection in the Human Prescription Drug category. It is labeled and distributed by Par Pharmaceutical, Inc.. The primary component is Ephedrine Sulfate.

Product ID42023-243_60a672cf-3914-4cab-ac1c-c511e00b05b8
NDC42023-243
Product TypeHuman Prescription Drug
Proprietary NameEPHEDRINE SULFATE
Generic NameEphedrine Sulfate
Dosage FormInjection
Route of AdministrationINTRAVENOUS
Marketing Start Date2021-01-31
Marketing CategoryNDA / NDA
Application NumberNDA213994
Labeler NamePar Pharmaceutical, Inc.
Substance NameEPHEDRINE SULFATE
Active Ingredient Strength5 mg/mL
Pharm Classesalpha-Adrenergic Agonist [EPC],Adrenergic alpha-Agonists [MoA],beta-Adrenergic Agonist [EPC],Adrenergic beta-Agonists [MoA],Norepinephrine Releasing Agent [EPC],Increased Norepinephrine Activity [PE]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 42023-243-01

10 mL in 1 VIAL, SINGLE-DOSE (42023-243-01)
Marketing Start Date2021-01-31
NDC Exclude FlagN
Sample Package?N

Drug Details

NDC Crossover Matching brand name "EPHEDRINE SULFATE" or generic name "Ephedrine Sulfate"

NDCBrand NameGeneric Name
0143-3145Ephedrine SulfateEphedrine Sulfate
0363-5789Ephedrine SulfateEphedrine Sulfate
0641-6238Ephedrine SulfateEphedrine Sulfate
0781-3269Ephedrine SulfateEphedrine Sulfate
14789-014Ephedrine SulfateEphedrine Sulfate
16714-037Ephedrine SulfateEphedrine Sulfate
17478-415Ephedrine SulfateEphedrine Sulfate
17478-515Ephedrine SulfateEphedrine Sulfate
17478-517Ephedrine SulfateEphedrine Sulfate
17478-955Ephedrine SulfateEphedrine Sulfate
42023-216Ephedrine SulfateEphedrine Sulfate
42023-243EPHEDRINE SULFATEEphedrine Sulfate
42023-253EPHEDRINE SULFATEEphedrine Sulfate
43598-725Ephedrine sulfateEphedrine sulfate
51662-1325EPHEDRINE SULFATEEPHEDRINE SULFATE
70121-1637Ephedrine SulfateEphedrine Sulfate
65219-257Ephedrine SulfateEphedrine Sulfate
42023-196CorphedraEphedrine Sulfate
42023-233Corphedraephedrine sulfate
14789-250EmerphedEphedrine Sulfate
© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.