TussiCaps

Product NDC
0187-0108
11-digit product format
001870108
Labeler code
0187
Product ID
0187-0108_7aae25b4-3cc1-4a2d-8bc6-666bdd86a252
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
hydrocodone polistirex and chlorpheniramine polistirex
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Bausch Health US LLC
Application
ANDA077273
Marketing category
ANDA
Marketing start
2011-09-02
Marketing end
0000-00-00
Substance
HYDROCODONE; CHLORPHENIRAMINE
Active strength
10 mg/1; mg/1
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
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0187-0108-01EA - Each0187-0108b704153f-b615-4888-9435-c65386ce6b3a12014-11-05
0187-0108-20EA - Each0187-01089e2e63de-9920-4139-b8c3-00648d1881db12014-11-05

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0187-0108-0100187010801100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0187-0108-01) 2011-09-020000-00-00NoNoCurrent
0187-0108-200018701082020 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (0187-0108-20) 2011-09-020000-00-00NoNoCurrent