MIDODRINE HYDROCHLORIDE

Product NDC
42291-616
11-digit product format
422910616
Labeler code
42291
Product ID
42291-616_6f3eea1e-d5c4-1854-e053-2a91aa0ae07b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
MIDODRINE HYDROCHLORIDE
Dosage form
TABLET
Route
ORAL
Labeler
AvKARE, Inc.
Application
ANDA076449
Marketing category
ANDA
Marketing start
2011-03-03
Marketing end
0000-00-00
Substance
MIDODRINE HYDROCHLORIDE
Active strength
5 mg/1
Pharmacologic classes
Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42291-616-90EA - Each42291-616d51d9b4b-891a-471d-ad01-df13c2f1ca6e12012-07-24