Siltussin SA

Product NDC
17856-0117
11-digit product format
178560117
Labeler code
17856
Product ID
17856-0117_ac983a67-c78b-4c21-9dae-357f460cd68b
Type
HUMAN OTC DRUG
Nonproprietary name
Guaifenesin
Dosage form
LIQUID
Route
ORAL
Labeler
Atlantic Biologicals Corps
Application
part341
Marketing category
OTC MONOGRAPH FINAL
Marketing start
1998-10-05
Marketing end
0000-00-00
Substance
GUAIFENESIN
Active strength
100 mg/5mL
NDC exclude flag
No
Listing certified through
2021-12-31
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
17856-0117-1ML - Milliliter17856-0117cdbfc206-63d3-4ba8-8c27-35cdb365af1b12016-05-16
17856-0117-2ML - Milliliter17856-0117f3421a93-2c6c-4e98-9f44-debc1e97c42812016-05-16
17856-0117-5ML - Milliliter17856-01176e85a1b2-2841-447a-a981-a9ace3fbdca412016-05-16

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
17856-0117-5178560117055 mL in 1 CUP (17856-0117-5) 5 ml2019-10-160000-00-00NoNoCurrent