Amoxicillin
- Product NDC
- 49999-983
- 11-digit product format
- 499990983
- Labeler code
- 49999
- Product ID
- 49999-983_0cbcd547-bfe9-427d-9f04-1b33757feab9
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA065325
- Marketing category
- ANDA
- Marketing start
- 2006-06-19
- Marketing end
- 2021-10-31
- Substance
- AMOXICILLIN
- Active strength
- 400 mg/5mL
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 49999-983-00 | 49999098300 | 100 mL in 1 BOTTLE (49999-983-00) | 100 ml | 2007-06-14 | 2021-10-31 | No | No | Current |