ephedrine sulfate
Generic: ephedrine sulfate
Labeler: lifestar pharma llcDrug Facts
Product Profile
Brand Name
ephedrine sulfate
Generic Name
ephedrine sulfate
Labeler
lifestar pharma llc
Dosage Form
INJECTION
Routes
Active Ingredients
ephedrine sulfate 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70756-611
Product ID
70756-611_abbedc8b-c9b5-4049-a31b-dbffb73c6556
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
70756611
Hyphenated Format
70756-611
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
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
- 25 VIAL, SINGLE-DOSE in 1 CARTON (70756-611-25) / 1 mL in 1 VIAL, SINGLE-DOSE (70756-611-82)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "abbedc8b-c9b5-4049-a31b-dbffb73c6556", "openfda": {"upc": ["0370756611820"], "unii": ["U6X61U5ZEG"], "rxcui": ["1116294"], "spl_set_id": ["49fc67d1-3b30-456b-951c-ca7f703432ab"], "manufacturer_name": ["Lifestar Pharma LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (70756-611-25) / 1 mL in 1 VIAL, SINGLE-DOSE (70756-611-82)", "package_ndc": "70756-611-25", "marketing_start_date": "20220415"}], "brand_name": "Ephedrine sulfate", "product_id": "70756-611_abbedc8b-c9b5-4049-a31b-dbffb73c6556", "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": "70756-611", "generic_name": "Ephedrine sulfate", "labeler_name": "Lifestar Pharma LLC", "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"}