FDA.reportPublic FDA data

Chlordiazepoxide Hydrochloride

Product NDC
43547-252
11-digit product format
435470252
Labeler code
43547
Product ID
43547-252_9653dfb9-2fe1-48e3-8b77-44f6eef703fa
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Chlordiazepoxide Hydrochloride
Dosage form
CAPSULE, GELATIN COATED
Route
ORAL
Labeler
Solco Healthcare US LLC
Application
ANDA085472
Marketing category
ANDA
Marketing start
2010-05-15
Marketing end
0000-00-00
Substance
CHLORDIAZEPOXIDE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Benzodiazepine [EPC],Benzodiazepines [CS]
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
632cace7-5e66-44d3-b8c3-9d6af8cdd96aProduct name520250623
6f1277d7-db3a-63fa-be84-d390d1482706Product name120140508

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
43547-252-10EA - Each43547-252ee5a1ba3-615a-497e-9cd0-7270c55a7a1c12012-07-24

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
905369chlordiazePOXIDE HCl 10 MG Oral CapsulePSN58113333-a25e-2cd0-e053-2991aa0a35ef1
905495chlordiazePOXIDE HCl 25 MG Oral CapsulePSN58113333-a25e-2cd0-e053-2991aa0a35ef1
905369chlordiazepoxide hydrochloride 10 MG Oral CapsuleSCD58113333-a25e-2cd0-e053-2991aa0a35ef1
905495chlordiazepoxide hydrochloride 25 MG Oral CapsuleSCD58113333-a25e-2cd0-e053-2991aa0a35ef1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
43547-252-1043547025210100 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (43547-252-10) 2010-05-150000-00-00NoNoCurrent