Amoxicillin
- Product NDC
- 68071-4693
- 11-digit product format
- 680714693
- Labeler code
- 68071
- Product ID
- 68071-4693_cb1c6290-4bd6-4205-e053-2a95a90ae87b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA065334
- Marketing category
- ANDA
- Marketing start
- 2006-12-28
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 400 mg/5mL
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68071-4693-5 | 68071469305 | 75 mL in 1 BOTTLE (68071-4693-5) | 75 ml | 2019-01-07 | 0000-00-00 | No | No | Current |