Amoxicillin
- Product NDC
- 50090-0288
- 11-digit product format
- 500900288
- Labeler code
- 50090
- Product ID
- 50090-0288_c2556ec7-aa40-43b4-823e-397cc974540a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065271
- Marketing category
- ANDA
- Marketing start
- 2005-11-09
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 250 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#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-0288-0 | 50090028800 | 30 CAPSULE in 1 BOTTLE (50090-0288-0) | 30 capsule | 2016-06-29 | 0000-00-00 | No | No | Current |
| 50090-0288-1 | 50090028801 | 21 CAPSULE in 1 BOTTLE (50090-0288-1) | 21 capsule | 2016-06-29 | 0000-00-00 | No | No | Current |
| 50090-0288-5 | 50090028805 | 15 CAPSULE in 1 BOTTLE (50090-0288-5) | 15 capsule | 2016-06-29 | 0000-00-00 | No | No | Current |