Neomycin Sulfate
- Product NDC
- 0527-1210
- 11-digit product format
- 005271210
- Labeler code
- 0527
- Product ID
- 0527-1210_f8be6f84-be1d-483a-aff2-fc1d0b3b4f68
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Neomycin Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lannett Company, Inc.
- Application
- ANDA204435
- Marketing category
- ANDA
- Marketing start
- 2016-06-10
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#