ADRENALIN (EPINEPHRINE) is a Intramuscular; Subcutaneous Injection in the Human Prescription Drug category. It is labeled and distributed by Hf Acquisition Co Llc, Dba Healthfirst. The primary component is Epinephrine.
Product ID | 51662-1290_7663c49d-1b1e-755d-e053-2991aa0a4ee3 |
NDC | 51662-1290 |
Product Type | Human Prescription Drug |
Proprietary Name | ADRENALIN (EPINEPHRINE) |
Generic Name | Adrenalin (epinephrine) |
Dosage Form | Injection |
Route of Administration | INTRAMUSCULAR; SUBCUTANEOUS |
Marketing Start Date | 2018-09-21 |
Marketing Category | NDA / NDA |
Application Number | NDA204200 |
Labeler Name | HF Acquisition Co LLC, DBA HealthFirst |
Substance Name | EPINEPHRINE |
Active Ingredient Strength | 1 mg/mL |
Pharm Classes | Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [CS] |
NDC Exclude Flag | N |
Listing Certified Through | 2019-12-31 |
Marketing Start Date | 2018-09-21 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | NDA |
Application Number | NDA204200 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2020-04-30 |
Marketing Category | NDA |
Application Number | NDA204200 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2018-09-21 |
Inactivation Date | 2020-01-31 |
Reactivation Date | 2020-02-07 |
Marketing Category | NDA |
Application Number | NDA204200 |
Product Type | HUMAN PRESCRIPTION DRUG |
Marketing Start Date | 2020-04-29 |
Ingredient | Strength |
---|---|
EPINEPHRINE | 1 mg/mL |
SPL SET ID: | 7663c49d-1b1d-755d-e053-2991aa0a4ee3 |
Manufacturer | |
UNII | |
RxNorm Concept Unique ID - RxCUI |