prazosin hydrochloride
Generic: prazosin hydrochloride
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
prazosin hydrochloride
Generic Name
prazosin hydrochloride
Labeler
remedyrepack inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
prazosin hydrochloride 1 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4457
Product ID
70518-4457_4af0abd0-77a6-d9c5-e063-6294a90a5499
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210971
Listing Expiration
2027-12-31
Marketing Start
2025-08-26
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184457
Hyphenated Format
70518-4457
Supplemental Identifiers
RxCUI
UNII
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
ANDA210971 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/1
Packaging
- 30 CAPSULE in 1 BLISTER PACK (70518-4457-0)
- 30 CAPSULE in 1 BLISTER PACK (70518-4457-1)
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "4af0abd0-77a6-d9c5-e063-6294a90a5499", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["312593"], "spl_set_id": ["fd860756-9b2e-4bfd-9063-bc4d26366fe6"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4457-0)", "package_ndc": "70518-4457-0", "marketing_start_date": "20250826"}, {"sample": false, "description": "30 CAPSULE in 1 BLISTER PACK (70518-4457-1)", "package_ndc": "70518-4457-1", "marketing_start_date": "20260215"}], "brand_name": "Prazosin Hydrochloride", "product_id": "70518-4457_4af0abd0-77a6-d9c5-e063-6294a90a5499", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70518-4457", "generic_name": "Prazosin Hydrochloride", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "1 mg/1"}], "application_number": "ANDA210971", "marketing_category": "ANDA", "marketing_start_date": "20250826", "listing_expiration_date": "20271231"}