hydromorphone hydrochloride

Generic: hydromorphone hydrochloride

Labeler: bryant ranch prepack
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name hydromorphone hydrochloride
Generic Name hydromorphone hydrochloride
Labeler bryant ranch prepack
Dosage Form TABLET
Routes
ORAL
Active Ingredients

hydromorphone hydrochloride 4 mg/1

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 71335-0723
Product ID 71335-0723_dd7057dd-4448-4f11-8c2d-6a1bfe0e1f50
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA205814
DEA Schedule cii
Listing Expiration 2026-12-31
Marketing Start 2016-05-17

Pharmacologic Class

Classes
full opioid agonists [moa] opioid agonist [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 713350723
Hyphenated Format 71335-0723

Supplemental Identifiers

RxCUI
897702
UNII
L960UP2KRW

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 hydromorphone hydrochloride (source: ndc)
Generic Name hydromorphone hydrochloride (source: ndc)
Application Number ANDA205814 (source: ndc)
Routes
ORAL
source: ndc

Resolved Composition

Strengths
  • 4 mg/1
source: ndc
Packaging
  • 90 TABLET in 1 BOTTLE (71335-0723-0)
  • 30 TABLET in 1 BOTTLE (71335-0723-1)
  • 180 TABLET in 1 BOTTLE (71335-0723-2)
  • 120 TABLET in 1 BOTTLE (71335-0723-3)
  • 20 TABLET in 1 BOTTLE (71335-0723-4)
  • 25 TABLET in 1 BOTTLE (71335-0723-5)
  • 100 TABLET in 1 BOTTLE (71335-0723-6)
  • 60 TABLET in 1 BOTTLE (71335-0723-7)
  • 56 TABLET in 1 BOTTLE (71335-0723-8)
  • 140 TABLET in 1 BOTTLE (71335-0723-9)
source: ndc

Packages (10)

71335-0723-0 90 TABLET in 1 BOTTLE (71335-0723-0) 71335-0723-1 30 TABLET in 1 BOTTLE (71335-0723-1) 71335-0723-2 180 TABLET in 1 BOTTLE (71335-0723-2) 71335-0723-3 120 TABLET in 1 BOTTLE (71335-0723-3) 71335-0723-4 20 TABLET in 1 BOTTLE (71335-0723-4) 71335-0723-5 25 TABLET in 1 BOTTLE (71335-0723-5) 71335-0723-6 100 TABLET in 1 BOTTLE (71335-0723-6) 71335-0723-7 60 TABLET in 1 BOTTLE (71335-0723-7) 71335-0723-8 56 TABLET in 1 BOTTLE (71335-0723-8) 71335-0723-9 140 TABLET in 1 BOTTLE (71335-0723-9)

Ingredients (1)

hydromorphone hydrochloride (4 mg/1)

Linked Drug Pages (1)

HYDROMORPHONE HYDROCHLORIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["ORAL"], "spl_id": "dd7057dd-4448-4f11-8c2d-6a1bfe0e1f50", "openfda": {"unii": ["L960UP2KRW"], "rxcui": ["897702"], "spl_set_id": ["29765ff0-3b1d-47da-953e-28bf0e6a56ef"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "90 TABLET in 1 BOTTLE (71335-0723-0)", "package_ndc": "71335-0723-0", "marketing_start_date": "20180416"}, {"sample": false, "description": "30 TABLET in 1 BOTTLE (71335-0723-1)", "package_ndc": "71335-0723-1", "marketing_start_date": "20180308"}, {"sample": false, "description": "180 TABLET in 1 BOTTLE (71335-0723-2)", "package_ndc": "71335-0723-2", "marketing_start_date": "20240809"}, {"sample": false, "description": "120 TABLET in 1 BOTTLE (71335-0723-3)", "package_ndc": "71335-0723-3", "marketing_start_date": "20240809"}, {"sample": false, "description": "20 TABLET in 1 BOTTLE (71335-0723-4)", "package_ndc": "71335-0723-4", "marketing_start_date": "20240809"}, {"sample": false, "description": "25 TABLET in 1 BOTTLE (71335-0723-5)", "package_ndc": "71335-0723-5", "marketing_start_date": "20240809"}, {"sample": false, "description": "100 TABLET in 1 BOTTLE (71335-0723-6)", "package_ndc": "71335-0723-6", "marketing_start_date": "20240809"}, {"sample": false, "description": "60 TABLET in 1 BOTTLE (71335-0723-7)", "package_ndc": "71335-0723-7", "marketing_start_date": "20180416"}, {"sample": false, "description": "56 TABLET in 1 BOTTLE (71335-0723-8)", "package_ndc": "71335-0723-8", "marketing_start_date": "20240809"}, {"sample": false, "description": "140 TABLET in 1 BOTTLE (71335-0723-9)", "package_ndc": "71335-0723-9", "marketing_start_date": "20240809"}], "brand_name": "HYDROMORPHONE HYDROCHLORIDE", "product_id": "71335-0723_dd7057dd-4448-4f11-8c2d-6a1bfe0e1f50", "dosage_form": "TABLET", "pharm_class": ["Full Opioid Agonists [MoA]", "Opioid Agonist [EPC]"], "product_ndc": "71335-0723", "dea_schedule": "CII", "generic_name": "HYDROMORPHONE HYDROCHLORIDE", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "HYDROMORPHONE HYDROCHLORIDE", "active_ingredients": [{"name": "HYDROMORPHONE HYDROCHLORIDE", "strength": "4 mg/1"}], "application_number": "ANDA205814", "marketing_category": "ANDA", "marketing_start_date": "20160517", "listing_expiration_date": "20261231"}