MUSE

Product NDC
0037-8120
11-digit product format
000378120
Labeler code
0037
Product ID
0037-8120_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
0000-00-00
Substance
ALPROSTADIL
Active strength
250 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
2023-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
0037-8120-062024-01-30C16284748780-11030e365-29df-111a-e063-dadaa90a10e24c55f3f9-c4cf-11df-851a-0800200c9a66
0037-8120-562024-01-30C16284748780-11030e365-29df-111a-e063-dadaa90a10e24c55f3f9-c4cf-11df-851a-0800200c9a66

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0037-8120-01EA - Each0037-8120679f1c9b-be34-411e-8f90-0c1828ec594512012-07-24
0037-8120-06EA - Each0037-812073d8e553-2ede-4737-86ef-5ccca783527112012-07-24

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0037-8120-06000378120066 POUCH in 1 CARTON (0037-8120-06) > 1 SUPPOSITORY in 1 POUCH (0037-8120-01) 6 pouch2011-07-220000-00-00NoNoCurrent
0037-8120-56000378120566 POUCH in 1 CARTON (0037-8120-56) > 1 SUPPOSITORY in 1 POUCH (0037-8120-01) 6 pouch2011-07-220000-00-00YesNoCurrent