rocuronium

Generic: rocuronium

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

Drug Facts

Product Profile

Brand Name rocuronium
Generic Name rocuronium
Labeler bryant ranch prepack
Dosage Form INJECTION, SOLUTION
Routes
INTRAVENOUS
Active Ingredients

rocuronium bromide 50 mg/5mL

Manufacturer
Bryant Ranch Prepack

Identifiers & Regulatory

Product NDC 72162-2263
Product ID 72162-2263_d6b8655a-04b5-46af-a453-0bf3fa8b8b25
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA210437
Listing Expiration 2027-12-31
Marketing Start 2020-07-20

Pharmacologic Class

Classes
neuromuscular nondepolarizing blockade [pe] nondepolarizing neuromuscular blocker [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 721622263
Hyphenated Format 72162-2263

Supplemental Identifiers

RxCUI
1234995
UNII
I65MW4OFHZ

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 rocuronium (source: ndc)
Generic Name rocuronium (source: ndc)
Application Number ANDA210437 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 50 mg/5mL
source: ndc
Packaging
  • 10 VIAL in 1 CARTON (72162-2263-2) / 5 mL in 1 VIAL
source: ndc

Packages (1)

Ingredients (1)

rocuronium bromide (50 mg/5mL)

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "d6b8655a-04b5-46af-a453-0bf3fa8b8b25", "openfda": {"unii": ["I65MW4OFHZ"], "rxcui": ["1234995"], "spl_set_id": ["6045ed5a-5d2c-4f17-aaba-458fbf87e85c"], "manufacturer_name": ["Bryant Ranch Prepack"]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (72162-2263-2)  / 5 mL in 1 VIAL", "package_ndc": "72162-2263-2", "marketing_start_date": "20240223"}], "brand_name": "Rocuronium", "product_id": "72162-2263_d6b8655a-04b5-46af-a453-0bf3fa8b8b25", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Neuromuscular Nondepolarizing Blockade [PE]", "Nondepolarizing Neuromuscular Blocker [EPC]"], "product_ndc": "72162-2263", "generic_name": "Rocuronium", "labeler_name": "Bryant Ranch Prepack", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Rocuronium", "active_ingredients": [{"name": "ROCURONIUM BROMIDE", "strength": "50 mg/5mL"}], "application_number": "ANDA210437", "marketing_category": "ANDA", "marketing_start_date": "20200720", "listing_expiration_date": "20271231"}