Oxacillin
- Product NDC
- 25021-163
- 11-digit product format
- 250210163
- Labeler code
- 25021
- Product ID
- 25021-163_d984ca46-02be-4252-8aec-818ec166eea0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- oxacillin sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Sagent Pharmaceuticals
- Application
- ANDA091245
- Marketing category
- ANDA
- Marketing start
- 2012-06-01
- Marketing end
- 0000-00-00
- Substance
- OXACILLIN SODIUM
- Active strength
- 10 g/100mL
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 25021-163 | OXACILLIN (OXACILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SAGENT PHARMACEUTICALS] | 10 | Legacy NDC | 20240712_9f0f30cb-ade2-4690-b63d-b069b8e4ed89.zip |
| 25021-163 | OXACILLIN (OXACILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [SAGENT PHARMACEUTICALS] | 2 | Legacy NDC | 20240712_fad9c5dc-be8e-436f-bb9b-dcbb41ae5db1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 25021-163-68 | 25021016368 | 10 BOTTLE in 1 CARTON (25021-163-68) > 100 mL in 1 BOTTLE | 10 bottle | 2018-10-15 | 0000-00-00 | No | No | Current |
| 25021-163-97 | 25021016397 | 1 BOTTLE in 1 CARTON (25021-163-97) > 100 mL in 1 BOTTLE | 1 bottle | 2020-06-01 | 0000-00-00 | No | No | Current |
| 25021-163-99 | 25021016399 | 10 BOTTLE in 1 CARTON (25021-163-99) > 100 mL in 1 BOTTLE | 10 bottle | 2012-06-01 | 0000-00-00 | No | No | Current |