Amoxicillin
- Product NDC
- 0143-9821
- 11-digit product format
- 001439821
- Labeler code
- 0143
- Product ID
- 0143-9821_e8bb6e15-4912-4ab8-a5d5-4ccede21853d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Hikma Pharmaceuticals USA Inc.
- Application
- ANDA205274
- Marketing category
- ANDA
- Marketing start
- 2021-07-31
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 125 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 0143-9821-01 | 00143982101 | 100 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (0143-9821-01) | 2021-07-31 | 0000-00-00 | No | No | Current |