prazosin hydrochloride
Generic: prazosin hydrochloride
Labeler: major pharmaceuticalsDrug Facts
Product Profile
Brand Name
prazosin hydrochloride
Generic Name
prazosin hydrochloride
Labeler
major pharmaceuticals
Dosage Form
CAPSULE
Routes
Active Ingredients
prazosin hydrochloride 5 mg/1
Manufacturer
Identifiers & Regulatory
Product NDC
0904-7022
Product ID
0904-7022_693144cc-ea54-4a3d-9938-9b4051a64f0b
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210971
Listing Expiration
2027-12-31
Marketing Start
2018-10-03
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
09047022
Hyphenated Format
0904-7022
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
- 5 mg/1
Packaging
- 100 BLISTER PACK in 1 CARTON (0904-7022-61) / 1 CAPSULE in 1 BLISTER PACK
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ORAL"], "spl_id": "693144cc-ea54-4a3d-9938-9b4051a64f0b", "openfda": {"unii": ["X0Z7454B90"], "rxcui": ["198141", "312593", "312594"], "spl_set_id": ["4f55f4db-dab3-4e50-9f71-5595fd3ccc12"], "manufacturer_name": ["Major Pharmaceuticals"]}, "finished": true, "packaging": [{"sample": false, "description": "100 BLISTER PACK in 1 CARTON (0904-7022-61) / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7022-61", "marketing_start_date": "20181003"}], "brand_name": "Prazosin Hydrochloride", "product_id": "0904-7022_693144cc-ea54-4a3d-9938-9b4051a64f0b", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0904-7022", "generic_name": "Prazosin Hydrochloride", "labeler_name": "Major Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA210971", "marketing_category": "ANDA", "marketing_start_date": "20181003", "listing_expiration_date": "20271231"}