Mupirocin
- Product NDC
- 70518-3774
- 11-digit product format
- 705183774
- Labeler code
- 70518
- Product ID
- 70518-3774_3b260cf6-0b89-c9b0-e063-6294a90a32d9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin Calcium
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA207116
- Marketing category
- ANDA
- Marketing start
- 2023-06-22
- Substance
- MUPIROCIN CALCIUM
- Active strength
- 20 mg/g
- Pharmacologic classes
- RNA Synthetase Inhibitor Antibacterial [EPC], RNA Synthetase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Mupirocin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MUPIROCIN CALCIUM | 20 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | RG38I2P540 |
| Rxcui | 311877 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-3774-0 | Mupirocin | 30 g in 1 TUBE | CREAM | 30 | | 3 |
| 70518-3774-0 | Mupirocin | 1 in 1 CARTON | CREAM | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-3774 | MUPIROCIN (MUPIROCIN CALCIUM) CREAM [REMEDYREPACK INC.] | 2 | Current NDC, 2 package rows | 20240331_9a1be092-6fe8-4b7c-a668-e584783f888b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-3774-0 | 70518377400 | 1 TUBE in 1 CARTON (70518-3774-0) / 30 g in 1 TUBE | 1 tube | 2023-06-22 | No | No | Historical |