Akovaz

Product NDC
76014-005
11-digit product format
760140005
Labeler code
76014
Product ID
76014-005_26f0bc51-fbc5-4d99-9972-6344f51f64a6
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ephedrine sulfate
Dosage form
INJECTION
Route
INTRAVENOUS
Labeler
Avadel Legacy Pharmaceuticals, LLC
Application
NDA208289
Marketing category
NDA
Marketing start
2016-08-01
Marketing end
2023-09-30
Substance
EPHEDRINE SULFATE
Active strength
50 mg/mL
Pharmacologic classes
alpha-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 flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
76014-005-25ML - Milliliter76014-0057ea61651-c238-420b-8f20-b18f4c127f7012016-06-14
76014-005-30ML - Milliliter76014-0059b613ebe-444f-4cc2-8c8c-2aa9793257a912017-12-14

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
76014-005-257601400052525 VIAL, SINGLE-DOSE in 1 CARTON (76014-005-25) > 1 mL in 1 VIAL, SINGLE-DOSE (76014-005-30) 2016-08-012023-09-30NoNoCurrent