Product Details for NDA 018053
BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
0.25%
Marketing Status: Discontinued
0.5%
Marketing Status: Discontinued
0.75%
Marketing Status: Discontinued
0.25%
Marketing Status: Discontinued
Active Ingredient: BUPIVACAINE HYDROCHLORIDE
Proprietary Name: BUPIVACAINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.25%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018053
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
Proprietary Name: BUPIVACAINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.25%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018053
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
0.5%
Marketing Status: Discontinued
Active Ingredient: BUPIVACAINE HYDROCHLORIDE
Proprietary Name: BUPIVACAINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.5%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018053
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
BUPIVACAINE HYDROCHLORIDE (BUPIVACAINE HYDROCHLORIDE)
Proprietary Name: BUPIVACAINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.5%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018053
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
0.75%
Marketing Status: Discontinued
Active Ingredient: BUPIVACAINE HYDROCHLORIDE
Proprietary Name: BUPIVACAINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.75%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018053
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: BUPIVACAINE HYDROCHLORIDE
Dosage Form; Route of Administration: INJECTABLE; INJECTION
Strength: 0.75%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N018053
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: HOSPIRA INC
Marketing Status: Discontinued
Patent and Exclusivity Information