Propranolol Hydrochloride

Product NDC
71335-0731
11-digit product format
713350731
Labeler code
71335
Product ID
71335-0731_bc4438ef-8ab3-4aa4-865f-b74c2fd4dd5b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
propranolol hydrochloride
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
NDA018553
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2017-12-21
Marketing end
0000-00-00
Substance
PROPRANOLOL HYDROCHLORIDE
Active strength
60 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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-0731-1EA - Each71335-0731ee85b1c4-59bf-4834-802f-d06e63997e2212020-01-03

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-0731-17133507310130 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0731-1) 2017-12-212023-06-30NoNoCurrent
71335-0731-27133507310218 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0731-2) 2017-12-212023-06-30NoNoCurrent
71335-0731-37133507310390 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0731-3) 2017-12-212023-06-30NoNoCurrent
71335-0731-47133507310428 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0731-4) 2018-03-192023-06-30NoNoCurrent
71335-0731-57133507310560 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0731-5) 2022-09-160000-00-00NoNoCurrent
71335-0731-67133507310610 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (71335-0731-6) 2022-09-160000-00-00NoNoCurrent