dihydroergotamine mesylate
Generic: dihydroergotamine mesylate
Labeler: baxter healthcare corporationDrug Facts
Product Profile
Brand Name
dihydroergotamine mesylate
Generic Name
dihydroergotamine mesylate
Labeler
baxter healthcare corporation
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
dihydroergotamine mesylate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
36000-300
Product ID
36000-300_f87dcd07-90ef-4e37-853e-7a5911a038b1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216747
Listing Expiration
2026-12-31
Marketing Start
2025-01-07
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
36000300
Hyphenated Format
36000-300
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
dihydroergotamine mesylate (source: ndc)
Generic Name
dihydroergotamine mesylate (source: ndc)
Application Number
ANDA216747 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 10 AMPULE in 1 CARTON (36000-300-10) / 1 mL in 1 AMPULE (36000-300-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "f87dcd07-90ef-4e37-853e-7a5911a038b1", "openfda": {"upc": ["0336000300018"], "unii": ["81AXN7R2QT"], "rxcui": ["861672"], "spl_set_id": ["f87dcd07-90ef-4e37-853e-7a5911a038b1"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 AMPULE in 1 CARTON (36000-300-10) / 1 mL in 1 AMPULE (36000-300-01)", "package_ndc": "36000-300-10", "marketing_start_date": "20250107"}], "brand_name": "dihydroergotamine mesylate", "product_id": "36000-300_f87dcd07-90ef-4e37-853e-7a5911a038b1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Ergotamine Derivative [EPC]", "Ergotamines [CS]"], "product_ndc": "36000-300", "generic_name": "dihydroergotamine mesylate", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "dihydroergotamine mesylate", "active_ingredients": [{"name": "DIHYDROERGOTAMINE MESYLATE", "strength": "1 mg/mL"}], "application_number": "ANDA216747", "marketing_category": "ANDA", "marketing_start_date": "20250107", "listing_expiration_date": "20261231"}