ATROPINE SULFATE
- Product NDC
- 71872-7246
- 11-digit product format
- 718727246
- Labeler code
- 71872
- Product ID
- 71872-7246_fa5960de-b896-25ae-e053-6394a90ac17f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATROPINE SULFATE
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Medical Purchasing Solutions, LLC
- Application
- NDA214652
- Marketing category
- NDA
- Marketing start
- 2021-01-11
- 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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 03J5ZE7KA5 | ATROPINE SULFATE | 5908-99-6 | ATROPINE SULFATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 71872-7246-1 | 71872724601 | 1 VIAL, SINGLE-DOSE in 1 BAG (71872-7246-1) / 1 mL in 1 VIAL, SINGLE-DOSE | 2021-03-30 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| ATROPINE SULFATE | Medical Purchasing Solutions, LLC | 2023-04-27 | HUMAN PRESCRIPTION DRUG LABEL | 2 |