Amoxicillin
- Product NDC
- 63629-7582
- 11-digit product format
- 636297582
- Labeler code
- 63629
- Product ID
- 63629-7582_bc1e8c6b-b67c-4460-b298-94b5075b6404
- 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
- 2023-12-31
- 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 |
|---|
| 63629-7582-1 | 63629758201 | 30 CAPSULE in 1 BOTTLE (63629-7582-1) | 30 capsule | 1994-09-30 | 0000-00-00 | No | No | Current |