MIDODRINE HYDROCHLORIDE

Product NDC
68151-2958
11-digit product format
681512958
Labeler code
68151
Product ID
68151-2958_59e8ac60-c215-4deb-92ff-d531f333cbb1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
MIDODRINE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
Carilion Materials Management
Application
ANDA076449
Marketing category
ANDA
Marketing start
2004-05-27
Marketing end
0000-00-00
Substance
MIDODRINE HYDROCHLORIDE
Active strength
5 mg/1
Pharmacologic classes
Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ee08dc62-0af6-bb42-639c-6cdc4aad4b08Product name620250801

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
68151-2958-02020-01-31C16284748780-19d75b9d0-4c1b-f424-e053-dadaa90a57ceMIDODRINE HYDROCHLORIDE TABLETS, 2.5 mg, 5 mg and 10 mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68151-2958-0MIDODRINE HYDROCHLORIDE1 in 1 PACKAGETABLET13

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68151-2958MIDODRINE HYDROCHLORIDE TABLET [CARILION MATERIALS MANAGEMENT]3Legacy NDC, 1 package rows20160805_9d5c58cc-1713-47ff-acbd-5b1fc79f9944.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
993470midodrine HCl 5 MG Oral TabletPSN9d5c58cc-1713-47ff-acbd-5b1fc79f99443
993470midodrine hydrochloride 5 MG Oral TabletSCD9d5c58cc-1713-47ff-acbd-5b1fc79f99443

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
68151-2958-0681512958001 in 1 PACKAGEHistorical