Nafcillin
- Product NDC
- 63323-328
- 11-digit product format
- 633230328
- Labeler code
- 63323
- Product ID
- 63323-328_89168d2d-2dc0-3f50-e053-2a95a90a31be
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- NAFCILLIN SODIUM
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Fresenius Kabi USA, LLC
- Application
- ANDA090002
- Marketing category
- ANDA
- Marketing start
- 2011-06-30
- 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 | 1721458, 1721460 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63323-328-20 | Nafcillin | 10 in 1 CARTON | INJECTION, POWDER, LYOPHILIZED, | 10 | | 5 |
| 63323-328-21 | Nafcillin | 8 mL in 1 VIAL | INJECTION, POWDER, LYOPHILIZED, | 8 | | 5 |
| 63323-328-22 | Nafcillin | 10 in 1 CARTON | INJECTION, POWDER, LYOPHILIZED, | 10 | | 4 |
| 63323-328-22 | Nafcillin | 8 mL in 1 VIAL | INJECTION, POWDER, LYOPHILIZED, | 8 | | 4 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63323-328 | NAFCILLIN (NAFCILLIN SODIUM) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [FRESENIUS KABI USA, LLC] | 5 | Current NDC, Legacy NDC, 2 package rows | 20190518_c39721a3-7b22-4720-9dbd-bc82f03d2af7.zip |
| 63323-328 | NAFCILLIN (NAFCILLIN SODIUM) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [FRESENIUS KABI USA, LLC] | 4 | Current NDC, Legacy NDC, 2 package rows | 20190525_3c2581a1-8051-4d7a-a1f7-521248648dc9.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 |
|---|
| 63323-328-20 | 63323032820 | 10 VIAL in 1 CARTON (63323-328-20) / 8 mL in 1 VIAL (63323-328-21) | 10 vial | 2011-06-30 | 0000-00-00 | No | No | Current |
| 63323-328-21 | 63323032821 | 8 mL in 1 VIAL | 8 ml | | | | | Historical |
| 63323-328-22 | 63323032822 | 10 VIAL in 1 CARTON (63323-328-22) / 8 mL in 1 VIAL | 10 vial | 2011-06-30 | 0000-00-00 | No | No | Current |