atropine sulfate
Generic: atropine sulfate
Labeler: remedyrepack inc.Drug Facts
Product Profile
Brand Name
atropine sulfate
Generic Name
atropine sulfate
Labeler
remedyrepack inc.
Dosage Form
INJECTION
Routes
Active Ingredients
atropine sulfate .4 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70518-4329
Product ID
70518-4329_402f9b6a-ab10-09d9-e063-6394a90a3edf
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA213561
Listing Expiration
2026-12-31
Marketing Start
2025-04-15
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
705184329
Hyphenated Format
70518-4329
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
atropine sulfate (source: ndc)
Generic Name
atropine sulfate (source: ndc)
Application Number
ANDA213561 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .4 mg/mL
Packaging
- 10 VIAL in 1 CARTON (70518-4329-0) / 20 mL in 1 VIAL (70518-4329-1)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["ENDOTRACHEAL", "INTRAMEDULLARY", "INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "402f9b6a-ab10-09d9-e063-6394a90a3edf", "openfda": {"unii": ["03J5ZE7KA5"], "rxcui": ["1190776"], "spl_set_id": ["8663ff94-8bea-4061-9fd5-3ab2e85e862e"], "manufacturer_name": ["REMEDYREPACK INC."]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL in 1 CARTON (70518-4329-0) / 20 mL in 1 VIAL (70518-4329-1)", "package_ndc": "70518-4329-0", "marketing_start_date": "20250415"}], "brand_name": "Atropine Sulfate", "product_id": "70518-4329_402f9b6a-ab10-09d9-e063-6394a90a3edf", "dosage_form": "INJECTION", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "70518-4329", "generic_name": "Atropine Sulfate", "labeler_name": "REMEDYREPACK INC.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atropine Sulfate", "active_ingredients": [{"name": "ATROPINE SULFATE", "strength": ".4 mg/mL"}], "application_number": "ANDA213561", "marketing_category": "ANDA", "marketing_start_date": "20250415", "listing_expiration_date": "20261231"}