Neomycin Sulfate
- Product NDC
- 0093-1177
- 11-digit product format
- 000931177
- Labeler code
- 0093
- Product ID
- 0093-1177_18e9e5b7-e08c-445e-86bb-90bc0953eda9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Neomycin Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Teva Pharmaceuticals USA, Inc.
- Application
- ANDA060304
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Substance
- NEOMYCIN SULFATE
- Active strength
- 500 mg/1
- Pharmacologic classes
- Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Neomycin Sulfate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NEOMYCIN SULFATE | 500 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 057Y626693 |
| Rxcui | 866042 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0093-1177-01 | Neomycin Sulfate | 100 in 1 BOTTLE | TABLET | 100 | | 12 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0093-1177 | NEOMYCIN SULFATE TABLET [TEVA PHARMACEUTICALS USA, INC.] | 12 | Current NDC, Legacy NDC, 1 package rows | 20230302_777dbfab-f83e-4738-ae1e-78619a9f82a7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0093-1177-01 | 00093117701 | 100 TABLET in 1 BOTTLE (0093-1177-01) | 100 tablet | 1990-09-30 | 0000-00-00 | No | No | Current |