nalbuphine hydrochloride

Generic: nalbuphine hydrochloride

Labeler: medical purchasing solutions, llc
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name nalbuphine hydrochloride
Generic Name nalbuphine hydrochloride
Labeler medical purchasing solutions, llc
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

nalbuphine hydrochloride 20 mg/mL

Manufacturer
Medical Purchasing Solutions, LLC

Identifiers & Regulatory

Product NDC 71872-7320
Product ID 71872-7320_28f280a2-70d3-6846-e063-6394a90afc82
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA070918
Listing Expiration 2026-12-31
Marketing Start 2005-05-16

Pharmacologic Class

Classes
competitive opioid antagonists [moa] opioid agonist/antagonist [epc] partial opioid agonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 718727320
Hyphenated Format 71872-7320

Supplemental Identifiers

RxCUI
904440
UNII
ZU4275277R

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 nalbuphine hydrochloride (source: ndc)
Generic Name nalbuphine hydrochloride (source: ndc)
Application Number ANDA070918 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • 20 mg/mL
source: ndc
Packaging
  • 1 CARTON in 1 BAG (71872-7320-1) / 1 VIAL, MULTI-DOSE in 1 CARTON / 10 mL in 1 VIAL, MULTI-DOSE
source: ndc

Packages (1)

71872-7320-1 1 CARTON in 1 BAG (71872-7320-1) / 1 VIAL, MULTI-DOSE in 1 CARTON / 10 mL in 1 VIAL, MULTI-DOSE

Ingredients (1)

nalbuphine hydrochloride (20 mg/mL)

Linked Drug Pages (1)

Nalbuphine Hydrochloride ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "28f280a2-70d3-6846-e063-6394a90afc82", "openfda": {"unii": ["ZU4275277R"], "rxcui": ["904440"], "spl_set_id": ["28f274a4-62c4-4e54-e063-6394a90a2200"], "manufacturer_name": ["Medical Purchasing Solutions, LLC"]}, "finished": true, "packaging": [{"sample": false, "description": "1 CARTON in 1 BAG (71872-7320-1)  / 1 VIAL, MULTI-DOSE in 1 CARTON / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "71872-7320-1", "marketing_start_date": "20231215"}], "brand_name": "Nalbuphine Hydrochloride", "product_id": "71872-7320_28f280a2-70d3-6846-e063-6394a90afc82", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Competitive Opioid Antagonists [MoA]", "Opioid Agonist/Antagonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "71872-7320", "generic_name": "NALBUPHINE HYDROCHLORIDE", "labeler_name": "Medical Purchasing Solutions, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Nalbuphine Hydrochloride", "active_ingredients": [{"name": "NALBUPHINE HYDROCHLORIDE", "strength": "20 mg/mL"}], "application_number": "ANDA070918", "marketing_category": "ANDA", "marketing_start_date": "20050516", "listing_expiration_date": "20261231"}