Amoxicillin
- Product NDC
- 68788-7160
- 11-digit product format
- 687887160
- Labeler code
- 68788
- Product ID
- 68788-7160_7cced498-a685-4ffc-81a5-18aeb6b46a39
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA065228
- Marketing category
- ANDA
- Marketing start
- 2005-07-13
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 875 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7160-2 | 68788716002 | 20 TABLET, FILM COATED in 1 BOTTLE (68788-7160-2) | 2018-06-04 | 0000-00-00 | No | No | Current |