Amoxicillin
- Product NDC
- 63629-4263
- 11-digit product format
- 636294263
- Labeler code
- 63629
- Product ID
- 63629-4263_794bd427-8c2a-415c-90a2-ab7c8383e009
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA064013
- Marketing category
- ANDA
- Marketing start
- 1993-01-01
- 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
- 2023-12-31
- 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 |
|---|
| 63629-4263-1 | 63629426301 | 30 TABLET, CHEWABLE in 1 BOTTLE (63629-4263-1) | 2022-06-17 | 0000-00-00 | No | No | Current |