NEOSTIGMINE METHYLSULFATE
- Product NDC
- 52584-057
- 11-digit product format
- 525840057
- Labeler code
- 52584
- Product ID
- 52584-057_59bc3396-90ff-478a-abb3-8def09a57180
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- neostigmine methylsulfate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- General Injectables and Vaccines, Inc.
- Application
- ANDA209933
- Marketing category
- ANDA
- Marketing start
- 2018-06-13
- Marketing end
- 2023-12-31
- Substance
- NEOSTIGMINE METHYLSULFATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [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 |
|---|
| 52584-057-00 | 52584005700 | 1 VIAL, MULTI-DOSE in 1 BAG (52584-057-00) > 10 mL in 1 VIAL, MULTI-DOSE | 2018-06-13 | 0000-00-00 | No | No | Current |