Oxacillin
- Product NDC
- 25021-162
- 11-digit product format
- 250210162
- Labeler code
- 25021
- Product ID
- 25021-162_d20bc39b-1c49-4dd7-8cde-2edcfe061c76
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxacillin sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA091246
- Marketing category
- ANDA
- Marketing start
- 2012-06-01
- Marketing end
- 0000-00-00
- Substance
- OXACILLIN SODIUM
- Active strength
- 2 g/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 25021-162 | OXACILLIN (OXACILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SAGENT PHARMACEUTICALS] | 9 | Legacy NDC | 20240724_f3bee4d7-82d8-4e2d-8fc8-4446e6fbf999.zip |
| 25021-162 | OXACILLIN (OXACILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SAGENT PHARMACEUTICALS] | 2 | Legacy NDC | 20240724_c4c9bc2d-fe19-4aca-8042-42394d3a3510.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 25021-162-24 | 25021016224 | 10 VIAL in 1 CARTON (25021-162-24) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 10 vial | 2012-06-01 | 0000-00-00 | No | No | Current |
| 25021-162-68 | 25021016268 | 10 VIAL in 1 CARTON (25021-162-68) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL | 10 vial | 2018-10-15 | 0000-00-00 | No | No | Current |