Propranolol Hydrochloride

Product NDC
55289-234
11-digit product format
552890234
Labeler code
55289
Product ID
55289-234_85a4e53d-fb78-c563-e053-2a91aa0a4be1
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Propranolol Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
PD-Rx Pharmaceuticals, Inc.
Application
ANDA078955
Marketing category
ANDA
Marketing start
2008-10-13
Marketing end
0000-00-00
Substance
PROPRANOLOL HYDROCHLORIDE
Active strength
40 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [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
55289-234-01EA - Each55289-2342293d421-5df0-4983-b9a9-8a80a62f852412013-02-13
55289-234-30EA - Each55289-234289a6f16-f5db-4cd1-bea2-9fd39cf8809512013-02-13
55289-234-90EA - Each55289-2348427e1ef-9e8b-4761-86c7-03487eb88cd312013-02-13