VERAPAMIL HYDROCHLORIDE tablet
Drug Labeling and Warnings
Drug Details [pdf]
- SPL UNCLASSIFIED
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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
NDC: 70771-1954-1 in bottles of 100 tablets
Verapamil Hydrochloride Extended-Release Tablets, USP 180 mg
100 Tablets
Rx Only
NDC: 70771-1955-1 in bottles of 100 tablets
Verapamil Hydrochloride Extended-Release Tablets, USP 240 mg
100 Tablets
Rx Only
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INGREDIENTS AND APPEARANCE
VERAPAMIL HYDROCHLORIDE
verapamil hydrochloride tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC: 70771-1953 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) VERAPAMIL HYDROCHLORIDE 120 mg Inactive Ingredients Ingredient Name Strength 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 Color BROWN (Beige) Score no score Shape OVAL Size 11mm Flavor Imprint Code 61;5 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 70771-1953-1 100 in 1 BOTTLE; Type 0: Not a Combination Product 05/21/2026 2 NDC: 70771-1953-5 500 in 1 BOTTLE; Type 0: Not a Combination Product 05/21/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA219252 05/21/2026 VERAPAMIL HYDROCHLORIDE
verapamil hydrochloride tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC: 70771-1954 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) VERAPAMIL HYDROCHLORIDE 180 mg Inactive Ingredients Ingredient Name Strength 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 Color BROWN (Beige) Score 2 pieces Shape OVAL Size 15mm Flavor Imprint Code 562 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 70771-1954-1 100 in 1 BOTTLE; Type 0: Not a Combination Product 05/21/2026 2 NDC: 70771-1954-5 500 in 1 BOTTLE; Type 0: Not a Combination Product 05/21/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA219252 05/21/2026 VERAPAMIL HYDROCHLORIDE
verapamil hydrochloride tabletProduct Information Product Type HUMAN PRESCRIPTION DRUG Item Code (Source) NDC: 70771-1955 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) VERAPAMIL HYDROCHLORIDE 240 mg Inactive Ingredients Ingredient Name Strength 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 Color BROWN (Beige) Score 2 pieces Shape OVAL (Capsule) Size 18mm Flavor Imprint Code 563 Contains Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC: 70771-1955-1 100 in 1 BOTTLE; Type 0: Not a Combination Product 05/21/2026 2 NDC: 70771-1955-5 500 in 1 BOTTLE; Type 0: Not a Combination Product 05/21/2026 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date ANDA ANDA219252 05/21/2026 Labeler - Zydus Lifesciences Limited (918596198) Registrant - Zydus Lifesciences Limited (677605858) Establishment Name Address ID/FEI Business Operations Zydus Lifesciences Limited 677605858 ANALYSIS(70771-1953, 70771-1954, 70771-1955) , MANUFACTURE(70771-1953, 70771-1954, 70771-1955)
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