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 2 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
68084-997
Product ID
68084-997_2b32cc04-a4d4-2cdd-e063-6394a90a2c85
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA071745
Listing Expiration
2026-12-31
Marketing Start
2018-05-11
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
68084997
Hyphenated Format
68084-997
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
- 2 mg/1
Packaging
- 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-997-01) / 1 CAPSULE in 1 BLISTER PACK (68084-997-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "2b32cc04-a4d4-2cdd-e063-6394a90a2c85", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["312593", "312594"], "spl_set_id": ["2b9f51fb-da48-4c81-b6b7-eb74b9cbaaf4"], "manufacturer_name": ["American Health Packaging"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-997-01) / 1 CAPSULE in 1 BLISTER PACK (68084-997-11)", "package_ndc": "68084-997-01", "marketing_start_date": "20180511"}], "brand_name": "Prazosin Hydrochloride", "product_id": "68084-997_2b32cc04-a4d4-2cdd-e063-6394a90a2c85", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "68084-997", "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": "2 mg/1"}], "application_number": "ANDA071745", "marketing_category": "ANDA", "marketing_start_date": "20180511", "listing_expiration_date": "20261231"}