FDA
Norepinephrine Bitartrate
The FDA lists this product in 19 strengths and forms.
Composition
- Active ingredients
- NOREPINEPHRINE BITARTRATE EQ 1MG BASE/ML
Strengths and forms
The FDA lists each strength of a product separately; these pages share one label.
- NOREPINEPHRINE BITARTRATE EQ 1MG BASE/ML · InjectableANDA218758-001 · Prescription
- NOREPINEPHRINE BITARTRATE EQ 1MG BASE/ML · InjectableANDA211980-001 · Discontinued
- NOREPINEPHRINE BITARTRATE EQ 1MG BASE/ML · InjectableANDA214455-001 · Prescription
- NOREPINEPHRINE BITARTRATE EQ 1MG BASE/ML · InjectableANDA219443-001 · Prescription
- NOREPINEPHRINE BITARTRATE EQ 1MG BASE/ML · InjectableANDA203662-001 · Prescription
- NOREPINEPHRINE BITARTRATE EQ 1MG BASE/ML · InjectableANDA214323-001 · Prescription
- NOREPINEPHRINE BITARTRATE EQ 1MG BASE/ML · InjectableANDA217575-001 · Prescription
- NOREPINEPHRINE BITARTRATE EQ 1MG BASE/ML · InjectableANDA040859-001 · Prescription
- NOREPINEPHRINE BITARTRATE EQ 1MG BASE/ML · InjectableANDA210839-001 · Prescription
- NOREPINEPHRINE BITARTRATE EQ 1MG BASE/ML · InjectableANDA040462-001 · Prescription
At a glance
- Brand name
- Norepinephrine Bitartrate
- Route
- Injection
- Dosage form
- Injectable
- Applicant
- Zydus Pharms
- Status
- Discontinued
- FDA approval
- 19 Jul 2022
- Application
- ANDA216341-001