atropine sulfate
Generic: atropine sulfate
Labeler: amneal pharmaceuticals llcDrug Facts
Product Profile
Brand Name
atropine sulfate
Generic Name
atropine sulfate
Labeler
amneal pharmaceuticals llc
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
atropine sulfate .1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70121-1705
Product ID
70121-1705_cd6e7dcc-16d0-4663-859e-c22fe300a536
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215342
Listing Expiration
2026-12-31
Marketing Start
2022-01-29
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
701211705
Hyphenated Format
70121-1705
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
atropine sulfate (source: ndc)
Generic Name
atropine sulfate (source: ndc)
Application Number
ANDA215342 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .1 mg/mL
Packaging
- 10 CARTON in 1 PACKAGE (70121-1705-7) / 1 SYRINGE, GLASS in 1 CARTON (70121-1705-1) / 5 mL in 1 SYRINGE, GLASS
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "cd6e7dcc-16d0-4663-859e-c22fe300a536", "openfda": {"upc": ["0370121170617"], "unii": ["03J5ZE7KA5"], "rxcui": ["1190546", "1190552"], "spl_set_id": ["80a31286-a741-4440-b200-290c08925d06"], "manufacturer_name": ["Amneal Pharmaceuticals LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 CARTON in 1 PACKAGE (70121-1705-7) / 1 SYRINGE, GLASS in 1 CARTON (70121-1705-1) / 5 mL in 1 SYRINGE, GLASS", "package_ndc": "70121-1705-7", "marketing_start_date": "20220129"}], "brand_name": "atropine sulfate", "product_id": "70121-1705_cd6e7dcc-16d0-4663-859e-c22fe300a536", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "70121-1705", "generic_name": "atropine sulfate", "labeler_name": "Amneal Pharmaceuticals LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "atropine sulfate", "active_ingredients": [{"name": "ATROPINE SULFATE", "strength": ".1 mg/mL"}], "application_number": "ANDA215342", "marketing_category": "ANDA", "marketing_start_date": "20220129", "listing_expiration_date": "20261231"}