Label: PROCHLORPERAZINE MALEATE tablet
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Contains inactivated NDC Code(s)
NDC Code(s): 51655-096-87 - Packager: Northwind Pharmaceuticals
- This is a repackaged label.
- Source NDC Code(s): 59746-113
- Category: HUMAN PRESCRIPTION DRUG LABEL
- DEA Schedule: None
- Marketing Status: Abbreviated New Drug Application
Drug Label Information
Updated April 28, 2014
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PRINCIPAL DISPLAY PANEL
NDC: 51655-096-87
MFG: 59746-113-06
Prochlorperazine Maleate 5MG
6 tablets
RX Only
Lot# NW09600001
Exp Date: 12/2015
Each tablet contains Prochlorperazine Maleate equivalent to 5mg Prochlorperazine
Dosage: See package insert
Store ar 68 to 77 degrees F.
Store in a tight, light resistant container (See USP). Keep out of reach of children.
Mfg by: Jubilant Cadista Pharmaceuticals Inc. Salisbury, MD 21801 USA Lot # 13P0651
Repackaged by Northwind Pharmaceuticals, Indianapolis, IN 46256
- WARNINGS AND PRECAUTIONS
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INGREDIENTS AND APPEARANCE
PROCHLORPERAZINE MALEATE
prochlorperazine maleate tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC:51655-096(NDC:59746-113) Route of Administration oral Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength PROCHLORPERAZINE MALEATE (UNII: I1T8O1JTL6) (PROCHLORPERAZINE - UNII:YHP6YLT61T) PROCHLORPERAZINE 5 mg in 6 Product Characteristics Color yellow Score no score Shape ROUND Size 7mm Flavor Imprint Code TL113 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51655-096-87 6 in 1 BOTTLE Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA040268 04/28/2014 Labeler - Northwind Pharmaceuticals (036986393) Registrant - Northwind Pharmaceuticals (036986393) Establishment Name Address ID/FEI Business Operations Northwind Pharmaceuticals 036986393 repack(51655-096)