OSCIMIN

Product NDC
68047-253
11-digit product format
680470253
Labeler code
68047
Product ID
68047-253_41495987-d924-1713-e063-6294a90a9235
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Hyoscyamine Sulfate
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
SUBLINGUAL
Labeler
Larken Laboratories, Inc.
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2011-08-03
Substance
HYOSCYAMINE SULFATE
Active strength
.125 mg/1
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
OSCIMIN
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
HYOSCYAMINE SULFATE.125 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
F2R8V82B84Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
1046982Internal RxNorm lookup
1652363Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2d5fa637-0696-40fe-9bc1-fcb6f07a50f6Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
a62a50ac-1535-4461-9768-8ae703e2e9fbProduct name120210525
9514609b-a2a9-f8ec-6ba6-3f8e5ee89877Product name120140508
bc07ef78-e82d-0c19-31f4-31f263780582Product name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
68047-253-01OSCIMIN100 in 1 BOTTLETABLET, ORALLY DISINTEGRATING10012

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68047-253-01EA - Each68047-2538aa56575-1685-42d5-98c3-7e7857ee8d0a12012-07-24

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
68047-253OSCIMIN (HYOSCYAMINE SULFATE) TABLET, ORALLY DISINTEGRATING [LARKEN LABORATORIES, INC.]11Current NDC, Legacy NDC, 1 package rows20241013_2d5fa637-0696-40fe-9bc1-fcb6f07a50f6.zip

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
OSCIMINHYOSCYAMINE SULFATELarken Laboratories, Inc.2d5fa637-0696-40fe-9bc1-fcb6f07a50f62025-10-16Warnings, Adverse reactionsExact identifier
ndc (product): 68047-253

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1046982hyoscyamine sulfate 0.125 MG Sublingual TabletPSN2d5fa637-0696-40fe-9bc1-fcb6f07a50f612
1652363OSCIMIN 0.125 MG Sublingual TabletPSN2d5fa637-0696-40fe-9bc1-fcb6f07a50f612
1652363hyoscyamine sulfate 0.125 MG Sublingual Tablet [Oscimin]SBD2d5fa637-0696-40fe-9bc1-fcb6f07a50f612
1046982hyoscyamine sulfate 0.125 MG Sublingual TabletSCD2d5fa637-0696-40fe-9bc1-fcb6f07a50f612
1046982hyoscyamine sulfate SL 0.125 Disintegrating Sublingual TabletSY2d5fa637-0696-40fe-9bc1-fcb6f07a50f612
1652363Oscimin 0.125 MG Sublingual TabletSY2d5fa637-0696-40fe-9bc1-fcb6f07a50f612

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
68047-253-0168047025301100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE (68047-253-01) 2011-08-030000-00-00NoNoCurrent