ISOXSUPRINE HYDROCHLORIDE

Product NDC: 42582-101
11-digit product format: 425820101
Labeler code: 42582
Product ID: 42582-101_a2344d62-64b9-4bd6-8f88-eef4e32897be
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: isoxsuprine hydrochloride
Dosage form: TABLET
Route: ORAL
Labeler: BI-COASTAL PHARMA INTERNATIONAL LIMITED LIABILITY COMPANY
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 2011-06-02
Marketing end: 0000-00-00
Substance: ISOXSUPRINE HYDROCHLORIDE
Active strength: 10 mg/1
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
42582-101-10	2020-03-03	C162847	48780-1	9d75b9d0-4ccc-f424-e053-dadaa90a57ce	18d6b14d-3ceb-4922-8d54-8c5b0fe23d7c
42582-101-10	2020-01-31	C162847	48780-1	9d75b9d0-4ccc-f424-e053-dadaa90a57ce	18d6b14d-3ceb-4922-8d54-8c5b0fe23d7c

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
42582-101-10	EA - Each	42582-101	ff04595c-02d8-4cce-8df9-a0c6dc99d6ce	1	2016-09-02

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
42582-101-10	42582010110	100 TABLET in 1 BOTTLE (42582-101-10)	100 tablet	2011-06-02	0000-00-00	No	No	Current