Ampicillin
- Product NDC
- 70594-085
- 11-digit product format
- 705940085
- Labeler code
- 70594
- Product ID
- 70594-085_2c29bd08-f467-4028-aac6-0a5b3007a5d3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- AMPICILLIN SODIUM
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- Xellia Pharmaceuticals USA LLC
- Application
- ANDA090583
- Marketing category
- ANDA
- Marketing start
- 2021-01-10
- Marketing end
- 0000-00-00
- Substance
- AMPICILLIN SODIUM
- Active strength
- 500 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70594-085 | AMPICILLIN (AMPICILLIN SODIUM) INJECTION, POWDER, FOR SOLUTION [XELLIA PHARMACEUTICALS USA LLC] | 2 | Legacy NDC | 20241212_94421dac-7865-49f8-ae52-871eee6465ac.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70594-085-02 | 70594008502 | 10 VIAL in 1 CARTON (70594-085-02) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (70594-085-01) | 10 vial | 2021-01-10 | 0000-00-00 | No | No | Current |