ATROPINE SULFATE
- Product NDC
- 0404-9819
- 11-digit product format
- 004049819
- Labeler code
- 0404
- Product ID
- 0404-9819_98bcd075-4fb0-4764-b1b2-91cb65c36b8a
- 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
- 2023-05-31
- 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
- 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 |
|---|
| 0404-9819-01 | 00404981901 | 1 VIAL, SINGLE-DOSE in 1 BAG (0404-9819-01) > 1 mL in 1 VIAL, SINGLE-DOSE | 2022-01-09 | 0000-00-00 | No | No | Current |