Dimercaptosuccinic Acid

Product NDC
51808-211
11-digit product format
518080211
Labeler code
51808
Product ID
51808-211_ec657ecb-6327-464c-8aab-6d61a0546b83
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Dimercaptosuccinic Acid
Dosage form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Labeler
AnazaoHealth Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2012-07-01
Marketing end
0000-00-00
Substance
2,3-DIMERCAPTOSUCCINIC ACID
Active strength
1 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c5cd4727-ac49-4409-82b1-5bd8006c3ec7Product name120171122

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51808-211-012019-11-27C16284748780-19855d018-deec-cd31-e053-dbdaa90ab51aDMSA (Dimercaptosuccinic acid)

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
51808-211-01Dimercaptosuccinic AcidDMSA1 in 1 KITINJECTION, POWDER, LYOPHILIZED,11

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51808-211DIMERCAPTOSUCCINIC ACID DMSA (DIMERCAPTOSUCCINIC ACID) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ANAZAOHEALTH CORPORATION]1Legacy NDC, 1 package rows20121203_5b11e596-3044-429b-9e48-33ba00946151.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
51808-211-01518080211011 in 1 KITHistorical