Atropine Sulfate

Product NDC: 71872-7100
Requested package NDC: 71872-7100-1
11-digit product format: 718727100
Labeler code: 71872
Product ID: 71872-7100_9ce57b9f-9718-91b1-e053-2995a90a100c
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Atropine Sulfate
Dosage form: INJECTION, SOLUTION
Route: INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
Labeler: Medical Purchasing Solutions, LLC
Marketing category: UNAPPROVED DRUG OTHER
Marketing start: 1992-12-01
Marketing end: 0000-00-00
Substance: ATROPINE SULFATE
Active strength: 1 mg/mL
Pharmacologic classes: Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
NDC exclude flag: No
Listing certified through: 2021-12-31
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	71872-7100	71872-7100-1	D	Discontinued by firm		2026-09-09

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 2 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Archive	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	71872-7100	71872-7100-1	D	Discontinued by firm		excluded / ndc_excluded.zip	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	71872-7100	71872-7100-1	D	Discontinued by firm		excluded / ndc_excluded.zip	`f5e01cc5f278…`	`a2eaf40c39c3…`

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
71872-7100	ATROPINE SULFATE INJECTION, SOLUTION [MEDICAL PURCHASING SOLUTIONS, LLC]	3	Legacy NDC	20230524_677bb6d6-7031-5be5-e053-2991aa0a5f6f.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
03J5ZE7KA5	ATROPINE SULFATE	5908-99-6	ATROPINE SULFATE

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
71872-7100-1	71872710001	1 VIAL, SINGLE-DOSE in 1 BAG (71872-7100-1) > 1 mL in 1 VIAL, SINGLE-DOSE	2018-03-05	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
ATROPINE SULFATE INJECTION, USP	Medical Purchasing Solutions, LLC	2023-05-23	HUMAN PRESCRIPTION DRUG LABEL	3

Atropine Sulfate

NDC auxiliary status#

Observed NDC auxiliary status history#

DailyMed Dashboard NDC Coverage#

Related Records#

Related UNII Ingredients#

Packages#

Related DailyMed Labels#