Amoxicillin
- Product NDC
- 63629-7589
- 11-digit product format
- 636297589
- Labeler code
- 63629
- Product ID
- 63629-7589_77209d91-ede0-48a2-9d9e-e4920aa97981
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA064076
- Marketing category
- ANDA
- Marketing start
- 1994-09-30
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 500 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 804826J2HU | AMOXICILLIN | 61336-70-7 | AMOXICILLIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7589-1 | 63629758901 | 40 CAPSULE in 1 BOTTLE (63629-7589-1) | 40 capsule | 2018-05-25 | 0000-00-00 | No | No | Current |