prazosin hydrochloride

Generic: prazosin hydrochloride

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

Drug Facts

Product Profile

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

prazosin hydrochloride 5 mg/1

Manufacturer
Granules Pharmaceuticals Inc.

Identifiers & Regulatory

Product NDC 70010-086
Product ID 70010-086_253979ce-5078-deec-e063-6294a90a5c52
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA214608
Listing Expiration 2026-12-31
Marketing Start 2022-01-03

Pharmacologic Class

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

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 70010086
Hyphenated Format 70010-086

Supplemental Identifiers

RxCUI
198141 312593 312594
UPC
0370010086012 0370010084018 0370010085015
UNII
X0Z7454B90

Packaging Origin

Original Packager
true

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 ANDA214608 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (70010-086-01)
  • 250 CAPSULE in 1 BOTTLE (70010-086-25)
source: ndc

Packages (2)

70010-086-01 100 CAPSULE in 1 BOTTLE (70010-086-01) 70010-086-25 250 CAPSULE in 1 BOTTLE (70010-086-25)

Ingredients (1)

prazosin hydrochloride (5 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": "253979ce-5078-deec-e063-6294a90a5c52", "openfda": {"upc": ["0370010086012", "0370010084018", "0370010085015"], "unii": ["X0Z7454B90"], "rxcui": ["198141", "312593", "312594"], "spl_set_id": ["d01b8927-a422-43b3-89de-088506fdee3c"], "manufacturer_name": ["Granules Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (70010-086-01)", "package_ndc": "70010-086-01", "marketing_start_date": "20220103"}, {"sample": false, "description": "250 CAPSULE in 1 BOTTLE (70010-086-25)", "package_ndc": "70010-086-25", "marketing_start_date": "20220103"}], "brand_name": "Prazosin Hydrochloride", "product_id": "70010-086_253979ce-5078-deec-e063-6294a90a5c52", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70010-086", "generic_name": "Prazosin Hydrochloride", "labeler_name": "Granules Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Prazosin Hydrochloride", "active_ingredients": [{"name": "PRAZOSIN HYDROCHLORIDE", "strength": "5 mg/1"}], "application_number": "ANDA214608", "marketing_category": "ANDA", "marketing_start_date": "20220103", "listing_expiration_date": "20261231"}