neostigmine methylsulfate
Generic: neostigmine methylsulfate
Labeler: fresenius kabi usa, llcDrug Facts
Product Profile
Brand Name
neostigmine methylsulfate
Generic Name
neostigmine methylsulfate
Labeler
fresenius kabi usa, llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
neostigmine methylsulfate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
65219-811
Product ID
65219-811_0831f9a8-b6ff-4b49-91ad-8177f968f543
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA203629
Listing Expiration
2026-12-31
Marketing Start
2015-01-08
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
65219811
Hyphenated Format
65219-811
Supplemental Identifiers
RxCUI
UPC
UNII
Packaging Origin
Original Packager
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
neostigmine methylsulfate (source: ndc)
Generic Name
neostigmine methylsulfate (source: ndc)
Application Number
NDA203629 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 VIAL, MULTI-DOSE in 1 TRAY (65219-811-10) / 10 mL in 1 VIAL, MULTI-DOSE (65219-811-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "0831f9a8-b6ff-4b49-91ad-8177f968f543", "openfda": {"upc": ["0365219811015"], "unii": ["98IMH7M386"], "rxcui": ["311936"], "spl_set_id": ["088f96eb-20b8-48f8-ac83-329f75a44ce1"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, MULTI-DOSE in 1 TRAY (65219-811-10) / 10 mL in 1 VIAL, MULTI-DOSE (65219-811-01)", "package_ndc": "65219-811-10", "marketing_start_date": "20230109"}], "brand_name": "Neostigmine Methylsulfate", "product_id": "65219-811_0831f9a8-b6ff-4b49-91ad-8177f968f543", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "65219-811", "generic_name": "Neostigmine Methylsulfate", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Neostigmine Methylsulfate", "active_ingredients": [{"name": "NEOSTIGMINE METHYLSULFATE", "strength": "1 mg/mL"}], "application_number": "NDA203629", "marketing_category": "NDA", "marketing_start_date": "20150108", "listing_expiration_date": "20261231"}