CYPROHEPTADINE HYDROCHLORIDE - cyproheptadine hydrochloride tablet 
Zydus Lifesciences Limited

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Cyproheptadine Hydrochloride Tablets, USP

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 70771-1076-1

Cyproheptadine Hydrochloride Tablets USP, 4 mg

100 Tablets

Rx only

label
CYPROHEPTADINE HYDROCHLORIDE 
cyproheptadine hydrochloride tablet
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1076
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
CYPROHEPTADINE HYDROCHLORIDE (UNII: NJ82J0F8QC) (CYPROHEPTADINE - UNII:2YHB6175DO) CYPROHEPTADINE HYDROCHLORIDE4 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
SODIUM STARCH GLYCOLATE TYPE A POTATO (UNII: 5856J3G2A2)  
Product Characteristics
ColorWHITE (White) Score2 pieces
ShapeROUND (Round) Size7mm
FlavorImprint Code 1110
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70771-1076-1100 in 1 BOTTLE; Type 0: Not a Combination Product07/20/2017
2NDC:70771-1076-01000 in 1 BOTTLE; Type 0: Not a Combination Product07/20/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA20893807/20/2017
Labeler - Zydus Lifesciences Limited (918596198)
Registrant - Zydus Lifesciences Limited (918596198)
Establishment
NameAddressID/FEIBusiness Operations
Zydus Lifesciences Limited863362789ANALYSIS(70771-1076) , MANUFACTURE(70771-1076)

Revised: 8/2022
Document Id: 63a07323-9908-4a23-84dd-94f2771e6a79
Set id: ccd7d3b2-b0c1-4f66-8d06-d21f5cfa8c1e
Version: 4
Effective Time: 20220804
 
Zydus Lifesciences Limited