BISACODYL

Product NDC
68784-102
11-digit product format
687840102
Labeler code
68784
Product ID
68784-102_c29c6c3c-e5cf-2f94-e053-2a95a90a1b41
Type
HUMAN OTC DRUG
Nonproprietary name
BISACODYL
Dosage form
SUPPOSITORY
Route
RECTAL
Labeler
Acino Products, LLC
Application
part334
Marketing category
OTC MONOGRAPH NOT FINAL
Marketing start
2005-01-01
Marketing end
0000-00-00
Substance
BISACODYL
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
68784-102-12EA - Each68784-102cbea6d32-e10f-4c6f-b3d4-c3d868f7cb1d12014-08-01

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
68784-102-0168784010201100 BLISTER PACK in 1 BOX (68784-102-01) > 1 SUPPOSITORY in 1 BLISTER PACK100 blister pack2021-05-180000-00-00NoNoCurrent
68784-102-08687840102088 BLISTER PACK in 1 BOX (68784-102-08) > 1 SUPPOSITORY in 1 BLISTER PACK8 blister pack2021-05-180000-00-00NoNoCurrent
68784-102-126878401021212 BLISTER PACK in 1 BOX (68784-102-12) > 1 SUPPOSITORY in 1 BLISTER PACK12 blister pack2021-05-180000-00-00NoNoCurrent
68784-102-166878401021616 BLISTER PACK in 1 BOX (68784-102-16) > 1 SUPPOSITORY in 1 BLISTER PACK16 blister pack2021-05-180000-00-00NoNoCurrent