Nafcillin
- Product NDC
- 55150-123
- 11-digit product format
- 551500123
- Labeler code
- 55150
- Product ID
- 55150-123_77c95416-c1d8-4955-b3b9-1aaefd761d60
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Nafcillin Sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Eugia US LLC
- Application
- ANDA091613
- Marketing category
- ANDA
- Marketing start
- 2012-12-26
- Substance
- NAFCILLIN SODIUM
- Active strength
- 2 g/8mL
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Nafcillin
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| NAFCILLIN SODIUM | 2 g/8mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 49G3001BCK |
| Rxcui | 1721460 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 55150-123-15 | Nafcillin | 8 mL in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 8 | | 13 |
| 55150-123-15 | Nafcillin | 10 in 1 BOX | INJECTION, POWDER, FOR SOLUTION | 10 | | 13 |
| 55150-123-16 | Nafcillin | 8 mL in 1 VIAL | INJECTION, POWDER, FOR SOLUTION | 8 | | 6 |
| 55150-123-16 | Nafcillin | 10 in 1 BOX | INJECTION, POWDER, FOR SOLUTION | 10 | | 6 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| NAFCILLIN SODIUM | ACTIVE INGREDIENT | 49G3001BCK | NAFCILLIN (NAFCILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [AUROMEDICS PHARMA LLC] | 5 | |
| NAFCILLIN | ACTIVE MOIETY | 4CNZ27M7RV | NAFCILLIN (NAFCILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [AUROMEDICS PHARMA LLC] | 5 | |
| SODIUM CITRATE | INACTIVE INGREDIENT | 1Q73Q2JULR | NAFCILLIN (NAFCILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [AUROMEDICS PHARMA LLC] | 5 | |
| NAFCILLIN SODIUM | ACTIVE INGREDIENT | 49G3001BCK | NAFCILLIN (NAFCILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [AUROMEDICS PHARMA LLC] | 1 | |
| NAFCILLIN | ACTIVE MOIETY | 4CNZ27M7RV | NAFCILLIN (NAFCILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [AUROMEDICS PHARMA LLC] | 1 | |
| SODIUM CITRATE | INACTIVE INGREDIENT | 1Q73Q2JULR | NAFCILLIN (NAFCILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [AUROMEDICS PHARMA LLC] | 1 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 55150-123 | NAFCILLIN (NAFCILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [EUGIA US LLC] | 12 | Current NDC, Legacy NDC, 2 package rows | 20240207_90717878-64cb-4ffc-90bc-7b4e81e3d1cd.zip |
| 55150-123 | NAFCILLIN (NAFCILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [EUGIA US LLC] | 5 | Current NDC, Legacy NDC, 2 package rows | 20230126_34821770-929c-40ea-a9e4-d4405dc869e1.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 |
|---|
| 55150-123-15 | 55150012315 | 10 VIAL in 1 BOX (55150-123-15) / 8 mL in 1 VIAL | 10 vial | 2012-12-26 | 0000-00-00 | No | No | Current |
| 55150-123-16 | 55150012316 | 10 VIAL in 1 BOX (55150-123-16) / 8 mL in 1 VIAL | 10 vial | 2012-12-26 | 0000-00-00 | No | No | Current |