atropine sulfate
Generic: atropine sulfate
Labeler: hf acquisition co. llc, dba health firstDrug Facts
Product Profile
Brand Name
atropine sulfate
Generic Name
atropine sulfate
Labeler
hf acquisition co. llc, dba health first
Dosage Form
INJECTION, SOLUTION
Routes
Active Ingredients
atropine sulfate .1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
51662-1207
Product ID
51662-1207_132c9ea8-2332-e63f-e063-6294a90ae8f1
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
UNAPPROVED DRUG OTHER
Listing Expiration
2026-12-31
Marketing Start
2018-08-22
Pharmacologic Class
Classes
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
516621207
Hyphenated Format
51662-1207
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)
Routes
source: ndc
Resolved Composition
Strengths
- .1 mg/mL
Packaging
- 1 SYRINGE, GLASS in 1 CARTON (51662-1207-1) / 10 mL in 1 SYRINGE, GLASS
- 10 POUCH in 1 CASE (51662-1207-3) / 1 CARTON in 1 POUCH (51662-1207-2) / 1 SYRINGE, GLASS in 1 CARTON / 10 mL in 1 SYRINGE, GLASS
Packages (2)
Ingredients (1)
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "132c9ea8-2332-e63f-e063-6294a90ae8f1", "openfda": {"unii": ["03J5ZE7KA5"], "rxcui": ["1190546"], "spl_set_id": ["74106ef7-83bf-47ba-e053-2991aa0aaec1"], "manufacturer_name": ["HF Acquisition Co. LLC, DBA Health First"]}, "finished": true, "packaging": [{"sample": false, "description": "1 SYRINGE, GLASS in 1 CARTON (51662-1207-1) / 10 mL in 1 SYRINGE, GLASS", "package_ndc": "51662-1207-1", "marketing_start_date": "20180822"}, {"sample": false, "description": "10 POUCH in 1 CASE (51662-1207-3) / 1 CARTON in 1 POUCH (51662-1207-2) / 1 SYRINGE, GLASS in 1 CARTON / 10 mL in 1 SYRINGE, GLASS", "package_ndc": "51662-1207-3", "marketing_start_date": "20180822"}], "brand_name": "ATROPINE SULFATE", "product_id": "51662-1207_132c9ea8-2332-e63f-e063-6294a90ae8f1", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "51662-1207", "generic_name": "ATROPINE SULFATE", "labeler_name": "HF Acquisition Co. LLC, DBA Health First", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATROPINE SULFATE", "active_ingredients": [{"name": "ATROPINE SULFATE", "strength": ".1 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20180822", "listing_expiration_date": "20261231"}