MUPIROCIN
- Product NDC
- 61919-203
- 11-digit product format
- 619190203
- Labeler code
- 61919
- Product ID
- 61919-203_5976580d-300f-4ad6-ac7c-bd2385d8f8ff
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- MUPIROCIN
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- DirectRX
- Application
- ANDA065123
- Marketing category
- ANDA
- Marketing start
- 2015-01-01
- Marketing end
- 0000-00-00
- Substance
- MUPIROCIN
- Active strength
- 20 mg/g
- Pharmacologic classes
- RNA Synthetase Inhibitor Antibacterial [EPC],RNA Synthetase Inhibitors [MoA]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 61919-203-22 | MUPIROCIN | 22 g in 1 TUBE | OINTMENT | 22 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 61919-203 | MUPIROCIN OINTMENT [DIRECTRX] | 1 | Legacy NDC, 1 package rows | 20151026_c1d0416b-4d94-4e00-bc53-1dca40afdf21.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 61919-203-22 | 61919020322 | 22 g in 1 TUBE | 22 g | Historical |