Midazolam hydrochloride

Product NDC
64679-765
11-digit product format
646790765
Labeler code
64679
Product ID
64679-765_209d926b-f1af-49e2-be94-53c7035b0b93
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Midazolam hydrochloride
Dosage form
INJECTION
Route
INTRAMUSCULAR; INTRAVENOUS
Labeler
Wockhardt USA LLC.
Application
ANDA078511
Marketing category
ANDA
Marketing start
2008-11-10
Marketing end
0000-00-00
Substance
MIDAZOLAM HYDROCHLORIDE
Active strength
5 mg/mL
Pharmacologic classes
Benzodiazepine [EPC],Benzodiazepines [CS]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#