Atropine Sulfate
- Product NDC
- 52584-630
- 11-digit product format
- 525840630
- Labeler code
- 52584
- Product ID
- 52584-630_103c5078-1b38-48fd-9417-e202336e489f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Atropine Sulfate
- Dosage form
- INJECTION, SOLUTION
- Route
- ENDOTRACHEAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- General Injectables & Vaccines, Inc.
- Application
- NDA021146
- Marketing category
- NDA
- Marketing start
- 2010-03-01
- Marketing end
- 2024-01-01
- 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 |
|---|
| 52584-630-05 | 52584063005 | 1 SYRINGE, PLASTIC in 1 BAG (52584-630-05) > 5 mL in 1 SYRINGE, PLASTIC | 2010-03-01 | 0000-00-00 | No | No | Current |