atropine sulfate
Generic: atropine sulfate
Labeler: somerset therapeutics, llcDrug Facts
Product Profile
Brand Name
atropine sulfate
Generic Name
atropine sulfate
Labeler
somerset therapeutics, llc
Dosage Form
SOLUTION
Routes
Active Ingredients
atropine sulfate .4 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
70069-631
Product ID
70069-631_7a8a5552-fe21-4d36-8396-b7c99f41b4c4
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
ANDA
Application Number
ANDA215969
Listing Expiration
2026-12-31
Marketing Start
2024-07-04
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
70069631
Hyphenated Format
70069-631
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
ANDA215969 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- .4 mg/mL
Packaging
- 25 VIAL in 1 CARTON (70069-631-25) / 1 mL in 1 VIAL (70069-631-01)
Packages (1)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "7a8a5552-fe21-4d36-8396-b7c99f41b4c4", "openfda": {"upc": ["0370069641255", "0370069631256", "0370069631010", "0370069641019"], "unii": ["03J5ZE7KA5"], "rxcui": ["1190795", "1666781"], "spl_set_id": ["a6fac578-c7bc-4b3c-a454-7889cc819118"], "manufacturer_name": ["Somerset Therapeutics, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "25 VIAL in 1 CARTON (70069-631-25) / 1 mL in 1 VIAL (70069-631-01)", "package_ndc": "70069-631-25", "marketing_start_date": "20240704"}], "brand_name": "Atropine Sulfate", "product_id": "70069-631_7a8a5552-fe21-4d36-8396-b7c99f41b4c4", "dosage_form": "SOLUTION", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "70069-631", "generic_name": "Atropine Sulfate", "labeler_name": "Somerset Therapeutics, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Atropine Sulfate", "active_ingredients": [{"name": "ATROPINE SULFATE", "strength": ".4 mg/mL"}], "application_number": "ANDA215969", "marketing_category": "ANDA", "marketing_start_date": "20240704", "listing_expiration_date": "20261231"}