VERAPAMIL HYDROCHLORIDE- verapamil hydrochloride tablet 
Zydus Lifesciences Limited

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Verapamil Hydrochloride Extended-Release Tablets, USP
Rx only

SPL UNCLASSIFIED

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 70771-1953-1 in bottles of 100 tablets

Verapamil Hydrochloride Extended-Release Tablets, USP 120 mg

100 Tablets

Rx Only

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NDC 70771-1954-1 in bottles of 100 tablets

Verapamil Hydrochloride Extended-Release Tablets, USP 180 mg

100 Tablets

Rx Only

image

NDC 70771-1955-1 in bottles of 100 tablets

Verapamil Hydrochloride Extended-Release Tablets, USP 240 mg

100 Tablets

Rx Only

image
VERAPAMIL HYDROCHLORIDE 
verapamil hydrochloride tablet
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1953
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) VERAPAMIL HYDROCHLORIDE120 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
SODIUM ALGINATE (UNII: C269C4G2ZQ)  
POVIDONE K30 (UNII: U725QWY32X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
TALC (UNII: 7SEV7J4R1U)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
ColorBROWN (Beige) Scoreno score
ShapeOVALSize11mm
FlavorImprint Code 61;5
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70771-1953-1100 in 1 BOTTLE; Type 0: Not a Combination Product05/21/2026
2NDC:70771-1953-5500 in 1 BOTTLE; Type 0: Not a Combination Product05/21/2026
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21925205/21/2026
VERAPAMIL HYDROCHLORIDE 
verapamil hydrochloride tablet
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1954
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) VERAPAMIL HYDROCHLORIDE180 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
SODIUM ALGINATE (UNII: C269C4G2ZQ)  
POVIDONE K30 (UNII: U725QWY32X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
TALC (UNII: 7SEV7J4R1U)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
ColorBROWN (Beige) Score2 pieces
ShapeOVALSize15mm
FlavorImprint Code 562
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70771-1954-1100 in 1 BOTTLE; Type 0: Not a Combination Product05/21/2026
2NDC:70771-1954-5500 in 1 BOTTLE; Type 0: Not a Combination Product05/21/2026
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21925205/21/2026
VERAPAMIL HYDROCHLORIDE 
verapamil hydrochloride tablet
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1955
Route of AdministrationORAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) VERAPAMIL HYDROCHLORIDE240 mg
Inactive Ingredients
Ingredient NameStrength
CELLULOSE, MICROCRYSTALLINE (UNII: OP1R32D61U)  
SODIUM ALGINATE (UNII: C269C4G2ZQ)  
POVIDONE K30 (UNII: U725QWY32X)  
MAGNESIUM STEARATE (UNII: 70097M6I30)  
HYPROMELLOSE 2910 (5 MPA.S) (UNII: R75537T0T4)  
TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
TALC (UNII: 7SEV7J4R1U)  
FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
FERRIC OXIDE RED (UNII: 1K09F3G675)  
Product Characteristics
ColorBROWN (Beige) Score2 pieces
ShapeOVAL (Capsule) Size18mm
FlavorImprint Code 563
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70771-1955-1100 in 1 BOTTLE; Type 0: Not a Combination Product05/21/2026
2NDC:70771-1955-5500 in 1 BOTTLE; Type 0: Not a Combination Product05/21/2026
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21925205/21/2026
Labeler - Zydus Lifesciences Limited (918596198)
Registrant - Zydus Lifesciences Limited (677605858)
Establishment
NameAddressID/FEIBusiness Operations
Zydus Lifesciences Limited677605858ANALYSIS(70771-1953, 70771-1954, 70771-1955) , MANUFACTURE(70771-1953, 70771-1954, 70771-1955)

Revised: 4/2026
Document Id: 75856e69-15d6-4982-895a-2c9e76e8020f
Set id: 051392d3-8ec1-450c-8c38-791d4ef1a2db
Version: 1
Effective Time: 20260409
 
Zydus Lifesciences Limited