Carbamazepine

Product NDC
0781-5988
11-digit product format
007815988
Labeler code
0781
Product ID
0781-5988_7a606a30-c4f8-4694-9642-edb8e3cf5eee
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Carbamazepine
Dosage form
TABLET, EXTENDED RELEASE
Route
ORAL
Labeler
Sandoz Inc
Application
NDA020234
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
1996-03-25
Marketing end
0000-00-00
Substance
CARBAMAZEPINE
Active strength
400 mg/1
Pharmacologic classes
Cytochrome P450 1A2 Inducers [MoA], Cytochrome P450 2B6 Inducers [MoA], Cytochrome P450 2C19 Inducers [MoA], Cytochrome P450 2C9 Inducers [MoA], Cytochrome P450 3A4 Inducers [MoA], Decreased Central Nervous System Disorganized Electrical Activity [PE], Mood Stabilizer [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0781-5988-01EA - Each0781-5988d7433cc3-afc5-4cfb-9b81-ef6dd7aeaa5112012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
0781-5988CARBAMAZEPINE ER (CARBAMAZEPINE) TABLET, EXTENDED RELEASE [SANDOZ INC]23Legacy NDC20221208_3a3344dc-9cc8-41da-859e-295d053597c1.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
0781-5988-0100781598801100 TABLET, EXTENDED RELEASE in 1 BOTTLE (0781-5988-01) 1996-03-250000-00-00NoNoCurrent