neostigmine methylsulfate
Generic: neostigmine methylsulfate
Labeler: sagent pharmaceuticalsDrug Facts
Product Profile
Brand Name
neostigmine methylsulfate
Generic Name
neostigmine methylsulfate
Labeler
sagent pharmaceuticals
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
neostigmine methylsulfate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
25021-611
Product ID
25021-611_bbd97c00-c7ad-4a28-86fd-4957d534e5ef
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA210652
Listing Expiration
2026-12-31
Marketing Start
2022-01-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
25021611
Hyphenated Format
25021-611
Supplemental Identifiers
RxCUI
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
ANDA210652 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 VIAL in 1 CARTON (25021-611-10) / 10 mL in 1 VIAL
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "bbd97c00-c7ad-4a28-86fd-4957d534e5ef", "openfda": {"unii": ["98IMH7M386"], "rxcui": ["311935", "311936"], "spl_set_id": ["3e07a5f7-8006-4011-9038-bc088cf55b8c"], "manufacturer_name": ["Sagent Pharmaceuticals"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (25021-611-10) / 10 mL in 1 VIAL", "package_ndc": "25021-611-10", "marketing_start_date": "20220115"}], "brand_name": "Neostigmine Methylsulfate", "product_id": "25021-611_bbd97c00-c7ad-4a28-86fd-4957d534e5ef", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "25021-611", "generic_name": "Neostigmine Methylsulfate", "labeler_name": "Sagent Pharmaceuticals", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Neostigmine Methylsulfate", "active_ingredients": [{"name": "NEOSTIGMINE METHYLSULFATE", "strength": "1 mg/mL"}], "application_number": "ANDA210652", "marketing_category": "ANDA", "marketing_start_date": "20220115", "listing_expiration_date": "20261231"}