Epinephrine

Product NDC
50090-2733
11-digit product format
500902733
Labeler code
50090
Product ID
50090-2733_aaeb2e08-e729-48ef-a6a4-8d4a66cf2e6d
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Epinephrine
Dosage form
INJECTION
Route
INTRAMUSCULAR
Labeler
A-S Medication Solutions
Application
NDA019430
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2016-12-15
Marketing end
0000-00-00
Substance
EPINEPHRINE
Active strength
0 mg/.3mL
Pharmacologic classes
Adrenergic alpha-Agonists [MoA],Adrenergic beta-Agonists [MoA],alpha-Adrenergic Agonist [EPC],beta-Adrenergic Agonist [EPC],Catecholamine [EPC],Catecholamines [CS]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50090-2733-02020-01-31C16284748780-19d75b9d1-0576-f424-e053-dadaa90a57ce1aa23ef5-7c23-45a3-b25f-a822ca1e679f

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-2733-0EA - Each50090-27334e180773-b927-4de6-aedc-27c45c03818512019-04-11