Neomycin Sulfate
- Product NDC
- 50383-565
- 11-digit product format
- 503830565
- Labeler code
- 50383
- Product ID
- 50383-565_a0fbf585-7be2-41be-95c1-7f0d5d5c1317
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Neomycin Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Hi-Tech Pharmacal Co. Inc.
- Application
- ANDA065220
- Marketing category
- ANDA
- Marketing start
- 2010-03-12
- 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
- 2021-12-31
- 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 |
|---|
| 50383-565-10 | 50383056510 | 100 TABLET in 1 BOTTLE, PLASTIC (50383-565-10) | 100 tablet | 2010-03-12 | 0000-00-00 | No | No | Current |