ephedrine sulfate
Generic: ephedrine sulfate
Labeler: propharma distributionDrug Facts
Product Profile
Brand Name
ephedrine sulfate
Generic Name
ephedrine sulfate
Labeler
propharma distribution
Dosage Form
INJECTION
Routes
Active Ingredients
ephedrine sulfate 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
84549-611
Product ID
84549-611_3a38b027-e8ea-5d08-e063-6294a90a3b49
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA216129
Listing Expiration
2026-12-31
Marketing Start
2022-04-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
84549611
Hyphenated Format
84549-611
Supplemental Identifiers
RxCUI
UNII
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
ephedrine sulfate (source: ndc)
Generic Name
ephedrine sulfate (source: ndc)
Application Number
ANDA216129 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 1 mL in 1 VIAL, SINGLE-DOSE (84549-611-25)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "3a38b027-e8ea-5d08-e063-6294a90a3b49", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["1116294"], "spl_set_id": ["3843c820-f54b-5349-e063-6294a90a6b18"], "manufacturer_name": ["ProPharma Distribution"]}, "finished": true, "packaging": [{"sample": false, "description": "1 mL in 1 VIAL, SINGLE-DOSE (84549-611-25)", "package_ndc": "84549-611-25", "marketing_start_date": "20250827"}], "brand_name": "Ephedrine sulfate", "product_id": "84549-611_3a38b027-e8ea-5d08-e063-6294a90a3b49", "dosage_form": "INJECTION", "pharm_class": ["Adrenergic alpha-Agonists [MoA]", "Adrenergic beta-Agonists [MoA]", "Increased Norepinephrine Activity [PE]", "Norepinephrine Releasing Agent [EPC]", "alpha-Adrenergic Agonist [EPC]", "beta-Adrenergic Agonist [EPC]"], "product_ndc": "84549-611", "generic_name": "Ephedrine sulfate", "labeler_name": "ProPharma Distribution", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ephedrine sulfate", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "50 mg/mL"}], "application_number": "ANDA216129", "marketing_category": "ANDA", "marketing_start_date": "20220415", "listing_expiration_date": "20261231"}