Atropine Sulfate
- Product NDC
- 0404-9821
- 11-digit product format
- 004049821
- Labeler code
- 0404
- Product ID
- 0404-9821_c67aae53-0480-4bbf-b3b9-d82b9c53537e
- 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
- 0000-00-00
- 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
- 2023-12-31
- 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 |
|---|
| 0404-9821-10 | 00404982110 | 1 SYRINGE, GLASS in 1 BAG (0404-9821-10) > 10 mL in 1 SYRINGE, GLASS | 2022-01-09 | 0000-00-00 | No | No | Current |