neostigmine methylsulfate
- Product NDC
- 72572-461
- 11-digit product format
- 725720461
- Labeler code
- 72572
- Product ID
- 72572-461_993286a1-6f76-459c-b18b-f4ade0526c43
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- neostigmine methylsulfate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Civica Inc.
- Application
- ANDA212512
- Marketing category
- ANDA
- Marketing start
- 2019-05-13
- Marketing end
- 0000-00-00
- Substance
- NEOSTIGMINE METHYLSULFATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC],Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 72572-461-24 | 72572046124 | 24 CARTON in 1 CARTON (72572-461-24) > 1 VIAL, MULTI-DOSE in 1 CARTON (72572-461-01) > 10 mL in 1 VIAL, MULTI-DOSE | 24 carton | 2019-05-13 | 0000-00-00 | No | No | Current |