Propranolol Hydrochloride

Product NDC
71335-1994
11-digit product format
713351994
Labeler code
71335
Product ID
71335-1994_b95ecc1f-0bfb-41a0-8334-92f807902dfd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Propranolol Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA070322
Marketing category
ANDA
Marketing start
2019-10-31
Substance
PROPRANOLOL HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
F8A3652H1VPROPRANOLOL HYDROCHLORIDE318-98-9PROPRANOLOL HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionUnitsMarketing startSampleExclude flagStatus
71335-1994-17133519940130 TABLET in 1 BOTTLE (71335-1994-1) 30 tablet2022-02-10NoNoHistorical
71335-1994-27133519940260 TABLET in 1 BOTTLE (71335-1994-2) 60 tablet2022-02-10NoNoHistorical
71335-1994-371335199403100 TABLET in 1 BOTTLE (71335-1994-3) 100 tablet2022-02-10NoNoHistorical
71335-1994-47133519940490 TABLET in 1 BOTTLE (71335-1994-4) 90 tablet2022-02-10NoNoHistorical
71335-1994-571335199405120 TABLET in 1 BOTTLE (71335-1994-5) 120 tablet2022-02-10NoNoHistorical
71335-1994-67133519940610 TABLET in 1 BOTTLE (71335-1994-6) 10 tablet2022-02-10NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
PROPRANOLOL HYDROCHLORIDE TABLETS, USPRxBryant Ranch Prepack2025-09-19HUMAN PRESCRIPTION DRUG LABEL102