Label: PROPRANOLOL HYROCHLORIDE- propranolol hydrochloride tablet
-
Contains inactivated NDC Code(s)
NDC Code(s): 51655-318-52 - Packager: Northwind Pharmaceuticals
- This is a repackaged label.
- Source NDC Code(s): 0378-0182
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated May 15, 2014
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
-
PRINCIPAL DISPLAY PANEL
NDC: 51655-318-52
MFG: 0378-0182-01
Propranolol HCL
10 MG
30 Tablets
Rx Only
Lot# NW32200001
Exp Date: 10/2015
Each tablet contains: Propranolol hydrochloride, USP...10mg
Dosage: See package insert
Store at 68 to 77 degrees F.
Store in a tight, light-resistant container (See USP). Keep out of the reach of children.
Mfg by: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA Lot# 3052270
Repackaged by: Northwind Pharmaceuticals, Indianapolis, IN 46256
- WARNINGS AND PRECAUTIONS
-
INGREDIENTS AND APPEARANCE
PROPRANOLOL HYROCHLORIDE
propranolol hydrochloride tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51655-318(NDC:0378-0182) Route of Administration oral Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PROPRANOLOL HYDROCHLORIDE (UNII: F8A3652H1V) (PROPRANOLOL - UNII:9Y8NXQ24VQ) PROPRANOLOL HYDROCHLORIDE 10 mg in 30 Product Characteristics Color orange Score 2 pieces Shape ROUND Size 6mm Flavor Imprint Code MYLAN;182;10 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51655-318-52 30 in 1 BOTTLE, DISPENSING Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA070213 05/15/2014 Labeler - Northwind Pharmaceuticals (036986393) Registrant - Northwind Pharmaceuticals (036986393) Establishment Name Address ID/FEI Business Operations Northwind Pharmaceuticals 036986393 repack(51655-318)