Product Details for NDA 017986
MINIZIDE (POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE)
0.5MG;EQ 1MG BASE
Marketing Status: Discontinued
0.5MG;EQ 2MG BASE
Marketing Status: Discontinued
0.5MG;EQ 5MG BASE
Marketing Status: Discontinued
0.5MG;EQ 1MG BASE
Marketing Status: Discontinued
Active Ingredient: POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE
Proprietary Name: MINIZIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 0.5MG;EQ 1MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017986
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
MINIZIDE (POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE)
Proprietary Name: MINIZIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 0.5MG;EQ 1MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017986
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
0.5MG;EQ 2MG BASE
Marketing Status: Discontinued
Active Ingredient: POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE
Proprietary Name: MINIZIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 0.5MG;EQ 2MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017986
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
MINIZIDE (POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE)
Proprietary Name: MINIZIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 0.5MG;EQ 2MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017986
Product Number: 002
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
0.5MG;EQ 5MG BASE
Marketing Status: Discontinued
Active Ingredient: POLYTHIAZIDE; PRAZOSIN HYDROCHLORIDE
Proprietary Name: MINIZIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 0.5MG;EQ 5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017986
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information
Proprietary Name: MINIZIDE
Dosage Form; Route of Administration: CAPSULE; ORAL
Strength: 0.5MG;EQ 5MG BASE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: N017986
Product Number: 003
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: PFIZER INC
Marketing Status: Discontinued
Patent and Exclusivity Information