NEOSTIGMINE METHYLSULFATE
Generic: neostigmine methylsulfate
Labeler: Henry Schein, Inc.Drug Facts
Product Profile
Brand Name
NEOSTIGMINE METHYLSULFATE
Generic Name
neostigmine methylsulfate
Labeler
Henry Schein, Inc.
Dosage Form
INJECTION
Routes
Active Ingredients
NEOSTIGMINE METHYLSULFATE 1 mg/mL
Identifiers & Regulatory
Product NDC
0404-9925
Product ID
0404-9925_ae929d69-7cc2-4ff8-86d2-15c3af1f6dca
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209933
Marketing Start
2022-01-13
Marketing End
2026-02-28
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
04049925
Hyphenated Format
0404-9925
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
ANDA209933 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 1 VIAL, MULTI-DOSE in 1 BAG (0404-9925-10) / 10 mL in 1 VIAL, MULTI-DOSE
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "ae929d69-7cc2-4ff8-86d2-15c3af1f6dca", "openfda": {"unii": ["98IMH7M386"], "rxcui": ["311936"], "spl_set_id": ["5f540e86-2a56-4cc0-8f69-64f051830a3d"], "manufacturer_name": ["Henry Schein, Inc."]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, MULTI-DOSE in 1 BAG (0404-9925-10) / 10 mL in 1 VIAL, MULTI-DOSE", "package_ndc": "0404-9925-10", "marketing_end_date": "20260228", "marketing_start_date": "20220113"}], "brand_name": "NEOSTIGMINE METHYLSULFATE", "product_id": "0404-9925_ae929d69-7cc2-4ff8-86d2-15c3af1f6dca", "dosage_form": "INJECTION", "pharm_class": ["Cholinesterase Inhibitor [EPC]", "Cholinesterase Inhibitors [MoA]"], "product_ndc": "0404-9925", "generic_name": "neostigmine methylsulfate", "labeler_name": "Henry Schein, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "NEOSTIGMINE METHYLSULFATE", "active_ingredients": [{"name": "NEOSTIGMINE METHYLSULFATE", "strength": "1 mg/mL"}], "application_number": "ANDA209933", "marketing_category": "ANDA", "marketing_end_date": "20260228", "marketing_start_date": "20220113"}