ATROPINE SULFATE
- Product NDC
- 0404-9990
- 11-digit product format
- 004049990
- Labeler code
- 0404
- Product ID
- 0404-9990_5db3983a-5133-43dd-a4cd-233387616c53
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- atropine sulfate injection
- Dosage form
- INJECTION
- Route
- ENDOTRACHEAL; INTRAMEDULLARY; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS
- Labeler
- Henry Schein, Inc.
- Application
- ANDA213561
- Marketing category
- ANDA
- Marketing start
- 2022-12-21
- 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0404-9990-20 | 00404999020 | 1 PACKAGE in 1 BAG (0404-9990-20) > 20 mL in 1 PACKAGE | 1 package | 2022-12-21 | 0000-00-00 | No | No | Current |