Amoxicillin
- Product NDC
- 72789-078
- 11-digit product format
- 727890078
- Labeler code
- 72789
- Product ID
- 72789-078_e9d5589d-8fb5-2d9f-e053-2a95a90a4e13
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Application
- ANDA062216
- Marketing category
- ANDA
- Marketing start
- 2019-04-03
- Marketing end
- 2022-10-01
- Substance
- AMOXICILLIN
- Active strength
- 500 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 | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72789-078-01 | 72789007801 | 100 CAPSULE in 1 BOTTLE, PLASTIC (72789-078-01) | 100 capsule | 2020-04-16 | 0000-00-00 | No | No | Current |
| 72789-078-82 | 72789007882 | 500 CAPSULE in 1 BOTTLE, PLASTIC (72789-078-82) | 500 capsule | 2020-04-16 | 0000-00-00 | No | No | Current |