Amoxicillin
- Product NDC
- 68788-9035
- 11-digit product format
- 687889035
- Labeler code
- 68788
- Product ID
- 68788-9035_2b49283b-51a4-4200-ad73-28b2a92c5fb3
- 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
- 2011-07-25
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 804826J2HU | AMOXICILLIN | 61336-70-7 | AMOXICILLIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-9035-1 | 68788903501 | 100 mL in 1 BOTTLE (68788-9035-1) | 100 ml | 2011-07-25 | 0000-00-00 | No | No | Current |