prazosin hydrochloride

Generic: prazosin hydrochloride

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

Drug Facts

Product Profile

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

prazosin hydrochloride 5 mg/1

Manufacturer
ANI Pharmaceuticals, Inc.

Identifiers & Regulatory

Product NDC 70954-021
Product ID 70954-021_48c81ece-bd52-4a98-a286-3fa5d594d854
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 70954021
Hyphenated Format 70954-021

Supplemental Identifiers

RxCUI
198141 312593 312594
UPC
0370954020202 0370954019503 0370954021100 0370954021209 0370954019206
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 ANDA210971 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 5 mg/1
source: ndc
Packaging
  • 100 CAPSULE in 1 BOTTLE (70954-021-10)
  • 250 CAPSULE in 1 BOTTLE (70954-021-20)
  • 100 BLISTER PACK in 1 CARTON (70954-021-40) / 1 CAPSULE in 1 BLISTER PACK (70954-021-30)
source: ndc

Packages (3)

70954-021-10 100 CAPSULE in 1 BOTTLE (70954-021-10) 70954-021-20 250 CAPSULE in 1 BOTTLE (70954-021-20) 70954-021-40 100 BLISTER PACK in 1 CARTON (70954-021-40) / 1 CAPSULE in 1 BLISTER PACK (70954-021-30)

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": "48c81ece-bd52-4a98-a286-3fa5d594d854", "openfda": {"upc": ["0370954020202", "0370954019503", "0370954021100", "0370954021209", "0370954019206"], "unii": ["X0Z7454B90"], "rxcui": ["198141", "312593", "312594"], "spl_set_id": ["35c7aa71-6171-4ba5-916c-384c28e5f5c1"], "manufacturer_name": ["ANI Pharmaceuticals, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "100 CAPSULE in 1 BOTTLE (70954-021-10)", "package_ndc": "70954-021-10", "marketing_start_date": "20181003"}, {"sample": false, "description": "250 CAPSULE in 1 BOTTLE (70954-021-20)", "package_ndc": "70954-021-20", "marketing_start_date": "20181003"}, {"sample": false, "description": "100 BLISTER PACK in 1 CARTON (70954-021-40)  / 1 CAPSULE in 1 BLISTER PACK (70954-021-30)", "package_ndc": "70954-021-40", "marketing_start_date": "20210413"}], "brand_name": "Prazosin Hydrochloride", "product_id": "70954-021_48c81ece-bd52-4a98-a286-3fa5d594d854", "dosage_form": "CAPSULE", "pharm_class": ["Adrenergic alpha-Antagonists [MoA]", "alpha-Adrenergic Blocker [EPC]"], "product_ndc": "70954-021", "generic_name": "Prazosin Hydrochloride", "labeler_name": "ANI Pharmaceuticals, Inc.", "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"}