Propranolol Hydrochloride

Product NDC
43478-903
11-digit product format
434780903
Labeler code
43478
Product ID
43478-903_54753570-5982-418f-acea-aabf39c8a50b
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
propranolol hydrochloride
Dosage form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Labeler
Rouses Point Pharm
Application
NDA018553
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2009-02-25
Marketing end
2019-09-30
Substance
PROPRANOLOL HYDROCHLORIDE
Active strength
160 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
43478-903-88EA - Each43478-903b923496a-8a4d-4374-bd07-97ab5c49469c12012-07-24