Tussionex Pennkinetic

Product NDC
50474-150
11-digit product format
504740150
Labeler code
50474
Product ID
50474-150_2c46faa3-aa31-4cfd-926d-8805a3149851
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
hydrocodone and chlorpheniramine
Dosage form
SUSPENSION, EXTENDED RELEASE
Route
ORAL
Labeler
UCB Inc.
Application
NDA019111
Marketing category
NDA
Marketing start
1987-12-31
Marketing end
2019-06-30
Substance
HYDROCODONE; CHLORPHENIRAMINE
Active strength
10 mg/5mL; mg/5mL
Pharmacologic classes
Opioid Agonist [EPC],Opioid Agonists [MoA],Histamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
DEA schedule
CII
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
50474-150-49ML - Milliliter50474-150fb209847-3afa-461d-a6b8-23222f7f200d12018-03-08