butorphanol tartrate

Generic: butorphanol tartrate

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

Drug Facts

Product Profile

Brand Name butorphanol tartrate
Generic Name butorphanol tartrate
Labeler hospira, inc.
Dosage Form INJECTION, SOLUTION
Routes
INTRAMUSCULAR INTRAVENOUS
Active Ingredients

butorphanol tartrate 2 mg/mL

Manufacturer
Hospira, Inc.

Identifiers & Regulatory

Product NDC 0409-1626
Product ID 0409-1626_280bcddf-00c7-4c78-a108-f86ce2d30f41
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA074626
DEA Schedule civ
Listing Expiration 2027-12-31
Marketing Start 2005-12-20

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 04091626
Hyphenated Format 0409-1626

Supplemental Identifiers

RxCUI
886627 1728351 1728355
UNII
2L7I72RUHN

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 butorphanol tartrate (source: ndc)
Generic Name butorphanol tartrate (source: ndc)
Application Number ANDA074626 (source: ndc)
Routes
INTRAMUSCULAR INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 2 mg/mL
source: ndc
Packaging
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1626-01) / 1 mL in 1 VIAL, SINGLE-DOSE (0409-1626-21)
  • 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1626-02) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-1626-42)
source: ndc

Packages (2)

0409-1626-01 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1626-01) / 1 mL in 1 VIAL, SINGLE-DOSE (0409-1626-21) 0409-1626-02 10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1626-02) / 2 mL in 1 VIAL, SINGLE-DOSE (0409-1626-42)

Ingredients (1)

butorphanol tartrate (2 mg/mL)

Linked Drug Pages (1)

Butorphanol Tartrate ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS"], "spl_id": "280bcddf-00c7-4c78-a108-f86ce2d30f41", "openfda": {"unii": ["2L7I72RUHN"], "rxcui": ["886627", "1728351", "1728355"], "spl_set_id": ["9822ca3f-aee2-46e5-8a96-495400e65d10"], "manufacturer_name": ["Hospira, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1626-01)  / 1 mL in 1 VIAL, SINGLE-DOSE (0409-1626-21)", "package_ndc": "0409-1626-01", "marketing_start_date": "20060317"}, {"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0409-1626-02)  / 2 mL in 1 VIAL, SINGLE-DOSE (0409-1626-42)", "package_ndc": "0409-1626-02", "marketing_start_date": "20051220"}], "brand_name": "Butorphanol Tartrate", "product_id": "0409-1626_280bcddf-00c7-4c78-a108-f86ce2d30f41", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Competitive Opioid Antagonists [MoA]", "Opioid Agonist/Antagonist [EPC]", "Partial Opioid Agonists [MoA]"], "product_ndc": "0409-1626", "dea_schedule": "CIV", "generic_name": "Butorphanol Tartrate", "labeler_name": "Hospira, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Butorphanol Tartrate", "active_ingredients": [{"name": "BUTORPHANOL TARTRATE", "strength": "2 mg/mL"}], "application_number": "ANDA074626", "marketing_category": "ANDA", "marketing_start_date": "20051220", "listing_expiration_date": "20271231"}