Propranolol Hydrochloride

Product NDC
49999-555
11-digit product format
499990555
Labeler code
49999
Product ID
49999-555_80466a35-888e-4ea2-a4bd-85eeb3b3629c
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Propranolol Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Lake Erie Medical DBA Quality Care Products LLC
Application
ANDA070176
Marketing category
ANDA
Marketing start
2012-03-23
Marketing end
0000-00-00
Substance
PROPRANOLOL HYDROCHLORIDE
Active strength
20 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

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
49999-555-14EA - Each49999-55555e7addd-a542-422f-8b62-c2484264e33812014-09-03
49999-555-30EA - Each49999-555731301b9-4431-4ce1-b1f8-e6972583b98912016-12-07
49999-555-60EA - Each49999-555a8d70c3f-4c6e-494e-9ac2-c00e02dacdd812013-02-13
49999-555-90EA - Each49999-5554581869b-8d2b-4e07-ab0d-f1e3bdadade012013-02-13