PROPRANOLOL HYDROCHLORIDE

Product NDC
65841-747
11-digit product format
658410747
Labeler code
65841
Product ID
65841-747_aa9c5856-379d-49b0-90b7-a16dc636d6d7
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
PROPRANOLOL HYDROCHLORIDE
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Zydus Lifesciences Limited
Application
ANDA090321
Marketing category
ANDA
Marketing start
2014-04-15
Marketing end
0000-00-00
Substance
PROPRANOLOL HYDROCHLORIDE
Active strength
120 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
65841-747-0165841074701100 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-747-01) 2014-04-150000-00-00NoNoCurrent
65841-747-0565841074705500 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-747-05) 2014-04-150000-00-00NoNoCurrent
65841-747-10658410747101000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-747-10) 2014-04-150000-00-00NoNoCurrent
65841-747-166584107471690 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (65841-747-16) 2014-04-150000-00-00NoNoCurrent
65841-747-7765841074777100 BLISTER PACK in 1 CARTON (65841-747-77) > 1 CAPSULE, EXTENDED RELEASE in 1 BLISTER PACK (65841-747-30) 100 blister pack2014-04-150000-00-00NoNoCurrent