Ampicillin
- Product NDC
- 70860-112
- 11-digit product format
- 708600112
- Labeler code
- 70860
- Product ID
- 70860-112_fde05a9c-6b34-4b37-8c94-203d1c439d67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ampicillin sodium
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Athenex Pharmaceutical Division, LLC.
- Application
- ANDA090354
- Marketing category
- ANDA
- Marketing start
- 2018-08-01
- Marketing end
- 0000-00-00
- Substance
- AMPICILLIN SODIUM
- Active strength
- 250 mg/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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70860-112-15 | 70860011215 | 10 VIAL in 1 CARTON (70860-112-15) > 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL (70860-112-41) | 10 vial | 2018-08-01 | 0000-00-00 | No | No | Current |