DILAUDID

Product NDC
59011-454
11-digit product format
590110454
Labeler code
59011
Product ID
59011-454_0cc002bd-a7e7-0cd0-bf27-678460984ad5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
HYDROMORPHONE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Purdue Pharma LP
Application
NDA019892
Marketing category
NDA
Marketing start
1956-01-01
Marketing end
0000-00-00
Substance
HYDROMORPHONE HYDROCHLORIDE
Active strength
4 mg/1
Pharmacologic classes
Full Opioid Agonists [MoA],Opioid Agonist [EPC]
DEA schedule
CII
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
59011-454-01EA - Each59011-454034cba53-0ad1-4772-b960-84d9ddbc5acb12012-07-24
59011-454-05EA - Each59011-454440bd93b-abc0-4812-a348-5922862b518a12012-07-24
59011-454-10EA - Each59011-454c6c1e5ed-bd41-461c-8567-321f4f03535912012-07-24