Amoxicillin
- Product NDC
- 68788-7812
- 11-digit product format
- 687887812
- Labeler code
- 68788
- Product ID
- 68788-7812_b375c593-5f19-4522-b1dc-53d796aff222
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA062216
- Marketing category
- ANDA
- Marketing start
- 2020-10-30
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 250 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7812-3 | 68788781203 | 30 CAPSULE in 1 BOTTLE, PLASTIC (68788-7812-3) | 30 capsule | 2020-10-30 | 0000-00-00 | No | No | Current |