Dicyclomine Hydrochloride

Product NDC
51079-119
11-digit product format
510790119
Labeler code
51079
Product ID
51079-119_9e02e57e-46d2-88ea-e053-2995a90a573e
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
dicyclomine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Mylan Institutional Inc.
Application
ANDA040317
Marketing category
ANDA
Marketing start
1998-03-06
Marketing end
2020-11-30
Substance
DICYCLOMINE HYDROCHLORIDE
Active strength
20 mg/1
Pharmacologic classes
Anticholinergic [EPC],Cholinergic Antagonists [MoA]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
51079-119-01EA - Each51079-11967cf0d0e-f2f3-4e9a-8c75-d61fafff18c312012-07-24
51079-119-20EA - Each51079-119f439cb31-c73e-49c9-b2eb-59779234954b12012-07-24