Dicyclomine

Product NDC: 55700-933
11-digit product format: 557000933
Labeler code: 55700
Product ID: 55700-933_28cdf7e1-6e68-4a35-8b03-66eb0c8cf6d4
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Dicyclomine hydrochloride
Dosage form: TABLET
Route: ORAL
Labeler: Quality Care Products, LLC
Application: ANDA040161
Marketing category: ANDA
Marketing start: 2021-08-31
Marketing end: 0000-00-00
Substance: DICYCLOMINE HYDROCHLORIDE
Active strength: 20 mg/1
Pharmacologic classes: Anticholinergic [EPC],Cholinergic Antagonists [MoA]
NDC exclude flag: No
Listing certified through: 2022-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
55700-933-90	2025-01-13	C162847	48780-1	1030e364-fe6a-111a-e063-dadaa90a10e2	c82c3ffb-f356-4467-9302-0efc1a4a9fb8
55700-933-90	2024-01-30	C162847	48780-1	1030e364-fe6a-111a-e063-dadaa90a10e2	c82c3ffb-f356-4467-9302-0efc1a4a9fb8

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
55700-933-90	EA - Each	55700-933	ec31c0b6-c7a5-4134-89ae-c7a492add8f1	1	2021-10-08

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
55700-933-90	55700093390	90 TABLET in 1 BOTTLE, PLASTIC (55700-933-90)	90 tablet	2021-08-31	0000-00-00	No	No	Current