ephedrine sulfate
Generic: ephedrine sulfate
Labeler: dr. reddy's laboratories, inc.Drug Facts
Product Profile
Brand Name
ephedrine sulfate
Generic Name
ephedrine sulfate
Labeler
dr. reddy's laboratories, inc.
Dosage Form
INJECTION
Routes
Active Ingredients
ephedrine sulfate 50 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
43598-725
Product ID
43598-725_e4f1e75a-e315-00f1-a044-13b6d2dcbca4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA212649
Listing Expiration
2026-12-31
Marketing Start
2021-10-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
43598725
Hyphenated Format
43598-725
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
ANDA212649 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 50 mg/mL
Packaging
- 25 VIAL, SINGLE-DOSE in 1 CARTON (43598-725-25) / 1 mL in 1 VIAL, SINGLE-DOSE (43598-725-11)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "e4f1e75a-e315-00f1-a044-13b6d2dcbca4", "openfda": {"unii": ["U6X61U5ZEG"], "rxcui": ["1116294"], "spl_set_id": ["1d1c41c1-8f5f-ee76-c890-4f1f2a3b2e96"], "manufacturer_name": ["Dr. Reddy's Laboratories, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL, SINGLE-DOSE in 1 CARTON (43598-725-25) / 1 mL in 1 VIAL, SINGLE-DOSE (43598-725-11)", "package_ndc": "43598-725-25", "marketing_start_date": "20211004"}], "brand_name": "Ephedrine sulfate", "product_id": "43598-725_e4f1e75a-e315-00f1-a044-13b6d2dcbca4", "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": "43598-725", "generic_name": "Ephedrine sulfate", "labeler_name": "Dr. Reddy's Laboratories, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ephedrine sulfate", "active_ingredients": [{"name": "EPHEDRINE SULFATE", "strength": "50 mg/mL"}], "application_number": "ANDA212649", "marketing_category": "ANDA", "marketing_start_date": "20211004", "listing_expiration_date": "20261231"}