Sulfacetamide Sodium

Product NDC
51672-1346
11-digit product format
516721346
Labeler code
51672
Product ID
51672-1346_ebca51fc-bda6-4932-8c37-4fd5e70dab5b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Sulfacetamide Sodium
Dosage form
SUSPENSION
Route
TOPICAL
Labeler
Taro Pharmaceuticals U.S.A., Inc.
Application
ANDA078668
Marketing category
ANDA
Marketing start
2009-05-20
Marketing end
0000-00-00
Substance
SULFACETAMIDE SODIUM
Active strength
100 mg/mL
Pharmacologic classes
Sulfonamide Antibacterial [EPC],Sulfonamides [CS]
NDC exclude flag
No
Listing certified through
2019-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51672-1346-82020-02-02C16284748780-19d75b9d0-93ca-f424-e053-dadaa90a57ce7d9135ec-ed8d-460b-8935-bf16dcf4a712
51672-1346-82020-01-31C16284748780-19d75b9d0-93ca-f424-e053-dadaa90a57ce7d9135ec-ed8d-460b-8935-bf16dcf4a712

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51672-1346-8ML - Milliliter51672-1346dbd4fbcd-4d6c-445d-8288-7b368fe5af7712012-07-24