Mupirocin
- Product NDC
- 0121-1076
- 11-digit product format
- 001211076
- Labeler code
- 0121
- Product ID
- 0121-1076_a43227b5-2dc1-40bf-a9cb-b564d480b897
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mupirocin
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Application
- ANDA065170
- Marketing category
- ANDA
- Marketing start
- 2026-03-13
- 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 |
|---|
| 0121-1076-00 | Mupirocin | 100 in 1 CARTON | OINTMENT | 100 | | 3 |
| 0121-1076-01 | Mupirocin | 1 g in 1 TUBE | OINTMENT | 1 | | 3 |
| 0121-1076-50 | Mupirocin | 50 in 1 CARTON | OINTMENT | 50 | | 3 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 0121-1076-00 | 00121107600 | 100 TUBE in 1 CARTON (0121-1076-00) / 1 g in 1 TUBE (0121-1076-01) | 100 tube | 2026-03-13 | No | No | Historical |
| 0121-1076-01 | 00121107601 | 1 g in 1 TUBE | 1 g | | | | Historical |
| 0121-1076-50 | 00121107650 | 50 TUBE in 1 CARTON (0121-1076-50) / 1 g in 1 TUBE (0121-1076-01) | 50 tube | 2026-03-13 | No | No | Historical |