Epinephrine

Product NDC
0517-1130
11-digit product format
005171130
Labeler code
0517
Product ID
0517-1130_9c0aad7a-46d5-4185-bfbd-ec11897d4bd8
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Epinephrine
Dosage form
INJECTION, SOLUTION
Route
INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Labeler
American Regent, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
1994-03-01
Marketing end
0000-00-00
Substance
EPINEPHRINE
Active strength
1 mg/mL
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
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0517-1130-052024-12-17C16284748780-1960f7f55-cdb5-8e05-e053-dbdaa90a074adaa651e5-40e1-4e87-9775-3f7cc44dff32
0517-1130-052019-10-29C16284748780-1960f7f55-cdb5-8e05-e053-dbdaa90a074adaa651e5-40e1-4e87-9775-3f7cc44dff32

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0517-1130-05ML - Milliliter0517-1130a2d5d09d-8b11-44e1-9af3-4196bea0ed2512012-07-24