ephedrine sulfate
Generic: ephedrine sulfate
Labeler: sandoz incDrug Facts
Product Profile
Brand Name
ephedrine sulfate
Generic Name
ephedrine sulfate
Labeler
sandoz inc
Dosage Form
INJECTION
Routes
Active Ingredients
ephedrine sulfate 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
0781-3269
Product ID
0781-3269_f923276f-a7dd-4940-9544-a71525cd5e1c
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA209784
Listing Expiration
2026-12-31
Marketing Start
2017-10-01
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
07813269
Hyphenated Format
0781-3269
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
ephedrine sulfate (source: ndc)
Generic Name
ephedrine sulfate (source: ndc)
Application Number
ANDA209784 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3269-95) / 1 mL in 1 VIAL, SINGLE-DOSE (0781-3269-71)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "f923276f-a7dd-4940-9544-a71525cd5e1c", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["1116294"], "spl_set_id": ["c8af7bb5-41da-4f8c-8acd-f489892a0d72"], "manufacturer_name": ["Sandoz Inc"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (0781-3269-95) / 1 mL in 1 VIAL, SINGLE-DOSE (0781-3269-71)", "package_ndc": "0781-3269-95", "marketing_start_date": "20171001"}], "brand_name": "Ephedrine Sulfate", "product_id": "0781-3269_f923276f-a7dd-4940-9544-a71525cd5e1c", "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": "0781-3269", "generic_name": "Ephedrine Sulfate", "labeler_name": "Sandoz Inc", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ephedrine Sulfate", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "50 mg/mL"}], "application_number": "ANDA209784", "marketing_category": "ANDA", "marketing_start_date": "20171001", "listing_expiration_date": "20261231"}