Hyoscyamine Sulfate

Product NDC
50532-115
11-digit product format
505320115
Labeler code
50532
Product ID
50532-115_5ae1ed10-3ec3-4a6d-bf30-7b8085d37757
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
HYOSCYAMINE SULFATE
Dosage form
TABLET
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
50532-115-102025-04-23C16284748780-19d75b9d0-b37a-f424-e053-dadaa90a57ce3a200492-c460-4b19-ac16-b64493904b88
50532-115-102020-01-31C16284748780-19d75b9d0-b37a-f424-e053-dadaa90a57ce3a200492-c460-4b19-ac16-b64493904b88

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50532-115-10EA - Each50532-115b2aeef34-7f7d-43e4-a7d5-b294d880c27912012-07-24