prazosin hydrochloride

Generic: prazosin hydrochloride

Labeler: nucare pharmaceuticals,inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name prazosin hydrochloride
Generic Name prazosin hydrochloride
Labeler nucare pharmaceuticals,inc.
Dosage Form CAPSULE
Routes
ORAL
Active Ingredients

prazosin hydrochloride 2 mg/1

Manufacturer
NuCare Pharmaceuticals,Inc.

Identifiers & Regulatory

Product NDC 68071-2972
Product ID 68071-2972_292cb35f-8034-23a8-e063-6294a90aef4c
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA215697
Listing Expiration 2026-12-31
Marketing Start 2023-01-03

Pharmacologic Class

Classes
adrenergic alpha-antagonists [moa] alpha-adrenergic blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 680712972
Hyphenated Format 68071-2972

Supplemental Identifiers

RxCUI
312594
UPC
0368071297218
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 ANDA215697 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 2 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (68071-2972-1)
source: ndc

Packages (1)

68071-2972-1 100 CAPSULE in 1 BOTTLE (68071-2972-1)

Ingredients (1)

prazosin hydrochloride (2 mg/1)

Linked Drug Pages (1)

prazosin hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "292cb35f-8034-23a8-e063-6294a90aef4c", "openfda": {"upc": ["0368071297218"], "unii": ["X0Z7454B90"], "rxcui": ["312594"], "spl_set_id": ["f8fd7e1d-471d-f4ae-e053-6294a90a8b41"], "manufacturer_name": ["NuCare Pharmaceuticals,Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (68071-2972-1)", "package_ndc": "68071-2972-1", "marketing_start_date": "20230410"}], "brand_name": "prazosin hydrochloride", "product_id": "68071-2972_292cb35f-8034-23a8-e063-6294a90aef4c", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "68071-2972", "generic_name": "prazosin hydrochloride", "labeler_name": "NuCare Pharmaceuticals,Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "prazosin hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "2 mg/1"}], "application_number": "ANDA215697", "marketing_category": "ANDA", "marketing_start_date": "20230103", "listing_expiration_date": "20261231"}