Dicyclomine Hydrochloride

Product NDC
0615-7755
11-digit product format
006157755
Labeler code
0615
Product ID
0615-7755_1b09fce6-6835-48ad-a2d3-aae80b549579
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Dicyclomine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
NCS HealthCare of KY, Inc dba Vangard Labs
Application
ANDA085223
Marketing category
ANDA
Marketing start
1986-07-30
Marketing end
0000-00-00
Substance
DICYCLOMINE HYDROCHLORIDE
Active strength
20 mg/1
Pharmacologic classes
Anticholinergic [EPC],Cholinergic Antagonists [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
0615-7755-392021-04-15C16284748780-19d75b9d0-dfc0-f424-e053-dadaa90a57ce47e1a332-823e-45cc-9f30-dfae8a1886dd
0615-7755-392020-01-31C16284748780-19d75b9d0-dfc0-f424-e053-dadaa90a57ce47e1a332-823e-45cc-9f30-dfae8a1886dd