Bethanechol Chloride

Product NDC: 64679-968
11-digit product format: 646790968
Labeler code: 64679
Product ID: 64679-968_31412d7a-affa-49a6-9144-a2d551847cba
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Bethanechol Chloride 50 mg
Dosage form: TABLET
Route: ORAL
Labeler: Wockhardt USA LLC.
Application: ANDA040518
Marketing category: ANDA
Marketing start: 2003-09-29
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: 2020-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
64679-968-01	2024-10-22	C162847	48780-1	e4f33bdf-ac1c-d8a0-e053-dadaa90a6e4e	8693204e-3bb5-4ada-93a4-eda563615db9
64679-968-01	2022-07-29	C162847	48780-1	e4f33bdf-ac1c-d8a0-e053-dadaa90a6e4e	8693204e-3bb5-4ada-93a4-eda563615db9

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
64679-968-01	EA - Each	64679-968	fb14cd84-ab51-40f3-8f86-8d1e48795af5	1	2012-07-24

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
64679-968-01	64679096801	100 TABLET in 1 BOTTLE (64679-968-01)	100 tablet	2003-09-29	0000-00-00	No	No	Current