Clonazepam

Product NDC
16714-752
11-digit product format
167140752
Labeler code
16714
Product ID
16714-752_e76a8afe-0b3b-4ec0-8a16-ccb4a7f15d29
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Clonazepam
Dosage form
TABLET
Route
ORAL
Labeler
Northstar RxLLC
Application
ANDA074979
Marketing category
ANDA
Marketing start
2016-07-01
Marketing end
2021-11-30
Substance
CLONAZEPAM
Active strength
1 mg/1
Pharmacologic classes
Benzodiazepine [EPC],Benzodiazepines [CS]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f8e2a02d-e7b1-29aa-eb39-98a679441d91Product name320190927
dc4336d1-53d4-d410-38d3-71aa2ce4749bProduct name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
16714-752-01EA - Each16714-7526235ec3f-e8d1-4d41-a49c-01d0e08b564a12018-03-08
16714-752-02EA - Each16714-7527b01bb1a-31cc-4820-b5e5-fa4c15adcac912018-07-03

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
197527clonazePAM 0.5 MG Oral TabletPSN1a55865b-6c6d-4974-bb0a-16788852d2681
197527clonazepam 0.5 MG Oral TabletSCD1a55865b-6c6d-4974-bb0a-16788852d2681