MUPIROCIN
- Product NDC
- 67296-2211
- 11-digit product format
- 672962211
- Labeler code
- 67296
- Product ID
- 67296-2211_49eb7298-0834-2baa-e063-6394a90a7b4a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MUPIROCIN
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Redpharm Drug
- Application
- ANDA217943
- Marketing category
- ANDA
- Marketing start
- 2025-05-16
- Substance
- MUPIROCIN
- Active strength
- 20 mg/g
- Pharmacologic classes
- RNA Synthetase Inhibitor Antibacterial [EPC], RNA Synthetase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- MUPIROCIN
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MUPIROCIN | 20 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | D0GX863OA5 |
| Rxcui | 106346 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-2211-1 | MUPIROCIN | 22 g in 1 TUBE | OINTMENT | 22 | | 1 |
| 67296-2211-1 | MUPIROCIN | 1 in 1 CARTON | OINTMENT | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 67296-2211-1 | 67296221101 | 1 TUBE in 1 CARTON (67296-2211-1) / 22 g in 1 TUBE | 1 tube | 2025-05-16 | No | No | Historical |