Amoxicillin
- Product NDC
- 68071-4696
- 11-digit product format
- 680714696
- Labeler code
- 68071
- Product ID
- 68071-4696_bb8bc3ff-1141-a08d-e053-2a95a90acac1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- Application
- ANDA061931
- Marketing category
- ANDA
- Marketing start
- 1990-09-30
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 125 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 |
|---|
| 68071-4696-5 | 68071469605 | 150 mL in 1 BOTTLE (68071-4696-5) | 150 ml | 2019-01-07 | 0000-00-00 | No | No | Current |