Neomycin Sulfate
- Product NDC
- 63629-8352
- 11-digit product format
- 636298352
- Labeler code
- 63629
- Product ID
- 63629-8352_1bd9745f-1e68-41ee-aba0-975c31de525c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Neomycin Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA060304
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Marketing end
- 0000-00-00
- Substance
- NEOMYCIN SULFATE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS]
- 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 |
|---|
| 63629-8352-1 | 63629835201 | 28 TABLET in 1 BOTTLE (63629-8352-1) | 28 tablet | 2020-09-02 | 0000-00-00 | No | No | Current |