Neostigmine Methylsulfate
- Product NDC
- 0641-6277
- 11-digit product format
- 006416277
- Labeler code
- 0641
- Product ID
- 0641-6277_f857cc8d-c0db-4dad-81ed-d863d2d206ae
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Neostigmine Methylsulfate
- Dosage form
- INJECTION
- Route
- INTRAVENOUS
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA207042
- Marketing category
- ANDA
- Marketing start
- 2015-12-28
- Substance
- NEOSTIGMINE METHYLSULFATE
- Active strength
- 1 mg/mL
- Pharmacologic classes
- Cholinesterase Inhibitor [EPC], Cholinesterase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 98IMH7M386 | NEOSTIGMINE METHYLSULFATE | 51-60-5 | NEOSTIGMINE METHYLSULFATE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 0641-6277-10 | 00641627710 | 10 VIAL, MULTI-DOSE in 1 CARTON (0641-6277-10) / 10 mL in 1 VIAL, MULTI-DOSE (0641-6277-01) | 2015-12-28 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Neostigmine Methylsulfate | Hikma Pharmaceuticals USA Inc. | 2024-04-09 | HUMAN PRESCRIPTION DRUG LABEL | 3 |