prazosin hydrochloride

Generic: prazosin hydrochloride

Labeler: remedyrepack inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prazosin hydrochloride
Generic Name prazosin hydrochloride
Labeler remedyrepack inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

prazosin hydrochloride 5 mg/1

Manufacturer
REMEDYREPACK INC.

Identifiers & Regulatory

Product NDC 70518-3352
Product ID 70518-3352_3a72c730-1c20-e2bf-e063-6294a90a3892
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA071745
Listing Expiration 2026-12-31
Marketing Start 2022-01-31

Pharmacologic Class

Classes
adrenergic alpha-antagonists [moa] alpha-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 705183352
Hyphenated Format 70518-3352

Supplemental Identifiers

RxCUI
198141
UNII
X0Z7454B90

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name prazosin hydrochloride (source: ndc)
Generic Name prazosin hydrochloride (source: ndc)
Application Number ANDA071745 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 POUCH in 1 BOX (70518-3352-0) / 1 CAPSULE in 1 POUCH (70518-3352-1)
source: ndc

Packages (1)

70518-3352-0 100 POUCH in 1 BOX (70518-3352-0) / 1 CAPSULE in 1 POUCH (70518-3352-1)

Ingredients (1)

prazosin hydrochloride (5 mg/1)

Linked Drug Pages (1)

Prazosin Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "3a72c730-1c20-e2bf-e063-6294a90a3892", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141"], "spl_set_id": ["a3045d80-33f4-4aab-8dce-42fbbf9d3ef7"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "100 POUCH in 1 BOX (70518-3352-0)  / 1 CAPSULE in 1 POUCH (70518-3352-1)", "package_ndc": "70518-3352-0", "marketing_start_date": "20220131"}], "brand_name": "Prazosin Hydrochloride", "product_id": "70518-3352_3a72c730-1c20-e2bf-e063-6294a90a3892", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70518-3352", "generic_name": "Prazosin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA071745", "marketing_category": "ANDA", "marketing_start_date": "20220131", "listing_expiration_date": "20261231"}