Amoxicillin
- Product NDC
- 50090-4260
- 11-digit product format
- 500904260
- Labeler code
- 50090
- Product ID
- 50090-4260_2d350bd4-b1ca-48de-bf3c-3b96278a1996
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065334
- Marketing category
- ANDA
- Marketing start
- 2006-12-28
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 200 mg/5mL
- 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4260-0 | 50090426000 | 100 mL in 1 BOTTLE (50090-4260-0) | 100 ml | 2019-04-10 | 0000-00-00 | No | No | Current |