prazosin hydrochloride
Generic: prazosin hydrochloride
Labeler: pd-rx pharmaceuticals, inc.Drug Facts
Product Profile
Brand Name
prazosin hydrochloride
Generic Name
prazosin hydrochloride
Labeler
pd-rx pharmaceuticals, inc.
Dosage Form
CAPSULE
Routes
Active Ingredients
prazosin hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
43063-248
Product ID
43063-248_41acda25-37c4-f94d-e063-6394a90a9a2d
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA072575
Listing Expiration
2026-12-31
Marketing Start
1989-02-28
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43063248
Hyphenated Format
43063-248
Supplemental Identifiers
RxCUI
UPC
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
ANDA072575 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 5 mg/1
Packaging
- 30 CAPSULE in 1 BOTTLE, PLASTIC (43063-248-30)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "41acda25-37c4-f94d-e063-6394a90a9a2d", "openfda": {"upc": ["0343063248300"], "unii": ["X0Z7454B90"], "rxcui": ["198141"], "spl_set_id": ["5d7dff44-84b1-4044-bc5a-c76ea11dd5a3"], "manufacturer_name": ["PD-Rx Pharmaceuticals, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "30 CAPSULE in 1 BOTTLE, PLASTIC (43063-248-30)", "package_ndc": "43063-248-30", "marketing_start_date": "20100520"}], "brand_name": "Prazosin Hydrochloride", "product_id": "43063-248_41acda25-37c4-f94d-e063-6394a90a9a2d", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "43063-248", "generic_name": "prazosin hydrochloride", "labeler_name": "PD-Rx Pharmaceuticals, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA072575", "marketing_category": "ANDA", "marketing_start_date": "19890228", "listing_expiration_date": "20261231"}