VERAPAMIL HYDROCHLORIDE - verapamil hydrochloride injection, solution 
Zydus Lifesciences Limited

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Verapamil Hydrochloride Injection, USP
Single-Dose Fliptop Vial
Protect from light.
Rx only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 70771-1601-1

Verapamil Hydrochloride Injection, USP

5 mg/2 mL

(2.5 mg/mL)

For Intravenous Use Only

Protect from light.

2 mL Single-Dose Vial 

Rx only

2 mL vial

NDC 70771-1601-5

Verapamil Hydrochloride Injection, USP

5 mg/2 mL

(2.5 mg/mL)

For Intravenous Use Only

Protect from light.

5 X 2 mL Single-Dose Vials 

Rx only

carton of 5 vials

NDC 70771-1601-7

Verapamil Hydrochloride Injection, USP

5 mg/2 mL

(2.5 mg/mL)

For Intravenous Use Only

Protect from light.

25 X 2 mL Single-Dose Vials 

Rx only

carton of 25 vials

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NDC 70771-1602-1

Verapamil Hydrochloride Injection, USP

10 mg/4 mL

(2.5 mg/mL)

For Intravenous Use Only

Protect from light.

4 mL Single-Dose Vial 

Rx only

4 mL vial

NDC 70771-1602-5

Verapamil Hydrochloride Injection, USP

10 mg/4 mL

(2.5 mg/mL)

For Intravenous Use Only

Protect from light.

5 X 4 mL Single-Dose Vials 

Rx only

carton of 5 vials
VERAPAMIL HYDROCHLORIDE 
verapamil hydrochloride injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1601
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) VERAPAMIL HYDROCHLORIDE2.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) 8.5 mg  in 1 mL
WATER (UNII: 059QF0KO0R)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70771-1601-725 in 1 CARTON10/22/2020
1NDC:70771-1601-55 in 1 CARTON
1NDC:70771-1601-12 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21421510/22/2020
VERAPAMIL HYDROCHLORIDE 
verapamil hydrochloride injection, solution
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:70771-1602
Route of AdministrationINTRAVENOUS
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
VERAPAMIL HYDROCHLORIDE (UNII: V3888OEY5R) (VERAPAMIL - UNII:CJ0O37KU29) VERAPAMIL HYDROCHLORIDE2.5 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
SODIUM CHLORIDE (UNII: 451W47IQ8X) 8.5 mg  in 1 mL
WATER (UNII: 059QF0KO0R)  
HYDROCHLORIC ACID (UNII: QTT17582CB)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:70771-1602-55 in 1 CARTON10/22/2020
1NDC:70771-1602-14 mL in 1 VIAL; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
ANDAANDA21421510/22/2020
Labeler - Zydus Lifesciences Limited (918596198)
Establishment
NameAddressID/FEIBusiness Operations
Zydus Lifesciences Limited873671928MANUFACTURE(70771-1601, 70771-1602) , ANALYSIS(70771-1601, 70771-1602)

Revised: 11/2022
Document Id: f1081c30-3025-42ce-b222-824630689bb8
Set id: cccf4a5f-6c5d-4d52-97e4-fe7a2dbd28d8
Version: 2
Effective Time: 20221105
 
Zydus Lifesciences Limited