Atropine Sulfate
- Product NDC
- 0404-9820
- 11-digit product format
- 004049820
- Labeler code
- 0404
- Product ID
- 0404-9820_32ad62c0-ccaa-4eb8-b748-ad1d73bc8464
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atropine Sulfate
- Dosage form
- INJECTION, SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Henry Schein, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2022-01-09
- Marketing end
- 2023-08-31
- Substance
- ATROPINE SULFATE
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Anticholinergic [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0404-9820-01 | 00404982001 | 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9820-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2022-01-09 | 2023-08-31 | No | No | Current |