Home NDC 71872-7037 Atropine Sulfate
Product NDC 71872-7037
11-digit product format 718727037
Labeler code 71872
Product ID 71872-7037_fd021c33-19cc-b7f5-e053-6394a90a9302
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name Atropine Sulfate
Dosage form INJECTION
Route INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Labeler Medical Purchasing Solutions, LLC
Marketing category UNAPPROVED DRUG OTHER
Marketing start 1971-01-01
Substance ATROPINE SULFATE
Active strength .4 mg/mL
Pharmacologic classes Anticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
NDC exclude flag No
Listing certified through 2026-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Atropine Sulfate
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength ATROPINE SULFATE .4 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 03J5ZE7KA5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1190776 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 71872-7037-1 Atropine Sulfate 1 in 1 BAG INJECTION 1 4 71872-7037-1 Atropine Sulfate 20 mL in 1 VIAL INJECTION 20 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 71872-7037 ATROPINE SULFATE INJECTION [MEDICAL PURCHASING SOLUTIONS, LLC] 4 Current NDC, Legacy NDC, 2 package rows 20230602_6bb51b79-ae86-aebf-e053-2991aa0a8d33.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 71872-7037-1 71872703701 1 VIAL in 1 BAG (71872-7037-1) / 20 mL in 1 VIAL 1 vial 2018-02-19 0000-00-00 No No Current