prazosin hydrochloride

Generic: prazosin hydrochloride

Labeler: major pharmaceuticals
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prazosin hydrochloride
Generic Name prazosin hydrochloride
Labeler major pharmaceuticals
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

prazosin hydrochloride 1 mg/1

Manufacturer
Major Pharmaceuticals

Identifiers & Regulatory

Product NDC 0904-7020
Product ID 0904-7020_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
adrenergic alpha-antagonists [moa] alpha-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09047020
Hyphenated Format 0904-7020

Supplemental Identifiers

RxCUI
198141 312593 312594
UNII
X0Z7454B90

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
ORAL
source: ndc

Resolved Composition

Strengths
  • 1 mg/1
source: ndc
Packaging
  • 100 BLISTER PACK in 1 CARTON (0904-7020-61) / 1 CAPSULE in 1 BLISTER PACK
source: ndc

Packages (1)

Ingredients (1)

prazosin hydrochloride (1 mg/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 (0904-7020-61)  / 1 CAPSULE in 1 BLISTER PACK", "package_ndc": "0904-7020-61", "marketing_start_date": "20181003"}], "brand_name": "Prazosin Hydrochloride", "product_id": "0904-7020_693144cc-ea54-4a3d-9938-9b4051a64f0b", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "0904-7020", "generic_name": "Prazosin Hydrochloride", "labeler_name": "Major Pharmaceuticals", "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": "20181003", "listing_expiration_date": "20271231"}