Amoxicillin
- Product NDC
- 55700-687
- 11-digit product format
- 557000687
- Labeler code
- 55700
- Product ID
- 55700-687_30cd9d58-2e43-4f86-9de9-2cf32b7302a2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, COATED
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA065255
- Marketing category
- ANDA
- Marketing start
- 2018-09-21
- Marketing end
- 2021-10-31
- Substance
- AMOXICILLIN
- Active strength
- 875 mg/1
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 55700-687-20 | 55700068720 | 20 TABLET, COATED in 1 BOTTLE (55700-687-20) | 2018-09-21 | 2021-10-31 | No | No | Current |