ISOXSUPRINE HYDROCHLORIDE

Product NDC
42582-200
11-digit product format
425820200
Labeler code
42582
Product ID
42582-200_44838a95-745c-4ee2-8361-e3fd9f3de1de
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
isoxsuprine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bi-Coastal Pharmaceutical Corporation
Marketing category
UNAPPROVED DRUG OTHER
Marketing start
2011-06-02
Marketing end
0000-00-00
Substance
ISOXSUPRINE HYDROCHLORIDE
Active strength
20 mg/1
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42582-200-10EA - Each42582-20083843715-f3e9-4595-9ea6-06b1e8c5e69d12013-06-04