DILAUDID

Product NDC
59011-452
11-digit product format
590110452
Labeler code
59011
Product ID
59011-452_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
2 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
59011-452-01EA - Each59011-452ec1cd6dc-2fb4-41db-8d17-e3a7b5f34a8e12012-07-24
59011-452-10EA - Each59011-45229c6ed32-5614-4033-95dc-931bc3a1bab212012-07-24