MUSE

Product NDC
0037-8110
11-digit product format
000378110
Labeler code
0037
Product ID
0037-8110_0209b68d-e74a-43a9-ad21-c9bca0293f0f
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Alprostadil
Dosage form
SUPPOSITORY
Route
URETHRAL
Labeler
Meda Pharmaceuticals Inc.
Application
NDA020700
Marketing category
NDA
Marketing start
2011-07-22
Marketing end
2022-04-30
Substance
ALPROSTADIL
Active strength
125 ug/1
Pharmacologic classes
Genitourinary Arterial Vasodilation [PE], Prostaglandin Analog [EPC], Prostaglandin E1 Agonist [EPC], Prostaglandin Receptor Agonists [MoA], Prostaglandins [CS], Venous Vasodilation [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
0037-8110-01EA - Each0037-8110fdc00518-7801-4b4e-bb7b-9963abb24b0d12012-07-24
0037-8110-06EA - Each0037-81103c0a4e50-8db3-49db-83c8-3e991eccbfb812012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0037-8110-06000378110066 POUCH in 1 CARTON (0037-8110-06) > 1 SUPPOSITORY in 1 POUCH (0037-8110-01) 6 pouch2011-07-222022-03-31NoNoCurrent
0037-8110-56000378110566 POUCH in 1 CARTON (0037-8110-56) > 1 SUPPOSITORY in 1 POUCH (0037-8110-01) 6 pouch2011-07-222022-04-30YesNoCurrent