Bethanechol Chloride

Product NDC: 0527-1329
11-digit product format: 005271329
Labeler code: 0527
Product ID: 0527-1329_747a1dfb-7e27-4592-8816-b2d91caa9012
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Bethanechol Chloride
Dosage form: TABLET
Route: ORAL
Labeler: Lannett Company, Inc.
Application: ANDA040677
Marketing category: ANDA
Marketing start: 2008-03-27
Marketing end: 0000-00-00
Substance: BETHANECHOL CHLORIDE
Active strength: 50 mg/1
Pharmacologic classes: Cholinergic Muscarinic Agonist [EPC], Cholinergic Muscarinic Agonists [MoA]
NDC exclude flag: No
Listing certified through: 2023-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
0527-1329-01	2024-01-30	C162847	48780-1	1030e365-1758-111a-e063-dadaa90a10e2	cb6a43e9-5663-47e1-8f77-ed4cb806436d

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0527-1329-01	EA - Each	0527-1329	87ee0748-05e4-4856-af28-8075aa51e4c7	1	2013-02-13

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
H4QBZ2LO84	BETHANECHOL CHLORIDE	590-63-6	BETHANECHOL CHLORIDE

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
0527-1329-01	00527132901	100 TABLET in 1 BOTTLE (0527-1329-01)	100 tablet	2008-03-27	0000-00-00	No	No	Current