atropine sulfate

Generic: atropine sulfate

Labeler: hf acquisition co llc, dba healthfirst
NDC Directory HUMAN PRESCRIPTION DRUG UNAPPROVED DRUG OTHER Inactive Finished

Drug Facts

Product Profile

Brand Name atropine sulfate
Generic Name atropine sulfate
Labeler hf acquisition co llc, dba healthfirst
Dosage Form INJECTION
Routes
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
Active Ingredients

atropine sulfate .4 mg/mL

Manufacturer
HF Acquisition Co LLC, DBA HealthFirst

Identifiers & Regulatory

Product NDC 51662-1311
Product ID 51662-1311_ae808675-c055-7f6c-e053-2995a90a5b49
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category UNAPPROVED DRUG OTHER
Listing Expiration 2026-12-31
Marketing Start 2018-10-06

Pharmacologic Class

Classes
anticholinergic [epc] cholinergic antagonists [moa] cholinergic muscarinic antagonist [epc] cholinergic muscarinic antagonists [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 516621311
Hyphenated Format 51662-1311

Supplemental Identifiers

RxCUI
1190776
UNII
03J5ZE7KA5

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
INTRAMUSCULAR INTRAVENOUS SUBCUTANEOUS
source: ndc

Resolved Composition

Strengths
  • .4 mg/mL
source: ndc
Packaging
  • 20 mL in 1 VIAL, MULTI-DOSE (51662-1311-1)
  • 25 POUCH in 1 CASE (51662-1311-3) / 1 mL in 1 POUCH (51662-1311-2)
source: ndc

Packages (2)

51662-1311-1 20 mL in 1 VIAL, MULTI-DOSE (51662-1311-1) 51662-1311-3 25 POUCH in 1 CASE (51662-1311-3) / 1 mL in 1 POUCH (51662-1311-2)

Ingredients (1)

atropine sulfate (.4 mg/mL)

Linked Drug Pages (1)

ATROPINE SULFATE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAMUSCULAR", "INTRAVENOUS", "SUBCUTANEOUS"], "spl_id": "ae808675-c055-7f6c-e053-2995a90a5b49", "openfda": {"unii": ["03J5ZE7KA5"], "rxcui": ["1190776"], "spl_set_id": ["77935b57-fcf6-c88a-e053-2a91aa0a0a80"], "manufacturer_name": ["HF Acquisition Co LLC, DBA HealthFirst"]}, "finished": true, "packaging": [{"sample": false, "description": "20 mL in 1 VIAL, MULTI-DOSE (51662-1311-1)", "package_ndc": "51662-1311-1", "marketing_start_date": "20181006"}, {"sample": false, "description": "25 POUCH in 1 CASE (51662-1311-3)  / 1 mL in 1 POUCH (51662-1311-2)", "package_ndc": "51662-1311-3", "marketing_start_date": "20200904"}], "brand_name": "ATROPINE SULFATE", "product_id": "51662-1311_ae808675-c055-7f6c-e053-2995a90a5b49", "dosage_form": "INJECTION", "pharm_class": ["Anticholinergic [EPC]", "Cholinergic Antagonists [MoA]", "Cholinergic Muscarinic Antagonist [EPC]", "Cholinergic Muscarinic Antagonists [MoA]"], "product_ndc": "51662-1311", "generic_name": "ATROPINE SULFATE", "labeler_name": "HF Acquisition Co LLC, DBA HealthFirst", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ATROPINE SULFATE", "active_ingredients": [{"name": "ATROPINE SULFATE", "strength": ".4 mg/mL"}], "marketing_category": "UNAPPROVED DRUG OTHER", "marketing_start_date": "20181006", "listing_expiration_date": "20261231"}