SODIUM HYDROXIDE

Product NDC
10481-3006
11-digit product format
104813006
Labeler code
10481
Product ID
10481-3006_b92631c2-5e63-4526-acdc-a2940145407b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
SODIUM HYDROXIDE
Dosage form
LIQUID
Route
TOPICAL
Labeler
Gordon Laboratories
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2010-07-16
Marketing end
0000-00-00
Substance
SODIUM HYDROXIDE
Active strength
0 g/g
Pharmacologic classes
Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10481-3006-12021-11-10C16284748780-1960f7f55-c7e5-8e05-e053-dbdaa90a074acb72936e-d185-4e18-8d59-01d07098c46b
10481-3006-12019-10-29C16284748780-1960f7f55-c7e5-8e05-e053-dbdaa90a074acb72936e-d185-4e18-8d59-01d07098c46b

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10481-3006-1ML - Milliliter10481-3006c2ea05fd-b088-49a2-bfbf-06b17b463ff612012-07-24