Amoxicillin
- Product NDC
- 68788-7318
- 11-digit product format
- 687887318
- Labeler code
- 68788
- Product ID
- 68788-7318_324c846f-67a2-4200-b00f-a7f9df3fe883
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065334
- Marketing category
- ANDA
- Marketing start
- 2019-01-16
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 400 mg/5mL
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7318-1 | 68788731801 | 100 mL in 1 BOTTLE (68788-7318-1) | 100 ml | 2019-01-16 | 0000-00-00 | No | No | Current |