prazosin hydrochloride
Generic: prazosin hydrochloride
Labeler: american health packagingDrug Facts
Product Profile
Brand Name
prazosin hydrochloride
Generic Name
prazosin hydrochloride
Labeler
american health packaging
Dosage Form
CAPSULE
Routes
Active Ingredients
prazosin hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
60687-572
Product ID
60687-572_2b330558-e654-74d6-e063-6394a90a9fd0
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA071745
Listing Expiration
2026-12-31
Marketing Start
2021-04-21
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
60687572
Hyphenated Format
60687-572
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
ANDA071745 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-572-32) / 1 CAPSULE in 1 BLISTER PACK (60687-572-33)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b330558-e654-74d6-e063-6394a90a9fd0", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141"], "spl_set_id": ["a2b84746-f780-4e21-adc9-62d09c9363cf"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-572-32) / 1 CAPSULE in 1 BLISTER PACK (60687-572-33)", "package_ndc": "60687-572-32", "marketing_start_date": "20210421"}], "brand_name": "Prazosin Hydrochloride", "product_id": "60687-572_2b330558-e654-74d6-e063-6394a90a9fd0", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "60687-572", "generic_name": "Prazosin Hydrochloride", "labeler_name": "American Health Packaging", "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": "20210421", "listing_expiration_date": "20261231"}