Hyoscyamine Sulfate SL

Product NDC
50532-113
11-digit product format
505320113
Labeler code
50532
Product ID
50532-113_02ab3cb8-eac0-4bf9-9c25-5ed1173bab93
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
HYOSCYAMINE SULFATE
Dosage form
TABLET, SOLUBLE
Route
ORAL
Labeler
Franklin Pharmaceutical LLC
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2010-05-01
Marketing end
0000-00-00
Substance
HYOSCYAMINE SULFATE
Active strength
0 mg/1
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
50532-113-102025-04-23C16284748780-19d75b9d0-5716-f424-e053-dadaa90a57cec5049243-5741-4d60-b65e-f3102fa7cc56
50532-113-102020-01-31C16284748780-19d75b9d0-5716-f424-e053-dadaa90a57cec5049243-5741-4d60-b65e-f3102fa7cc56

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50532-113-10EA - Each50532-11346c1990c-4ebd-4de2-b407-d32c2b4254df12012-07-24