Amoxicillin
- Product NDC
- 70934-140
- 11-digit product format
- 709340140
- Labeler code
- 70934
- Product ID
- 70934-140_d20376d1-5c2a-db22-e053-2a95a90a717d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, CHEWABLE
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA064013
- Marketing category
- ANDA
- Marketing start
- 2019-12-23
- 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 |
|---|
| 70934-140-30 | 70934014030 | 30 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (70934-140-30) | 2018-06-25 | 0000-00-00 | No | No | Current |
| 70934-140-40 | 70934014040 | 40 TABLET, CHEWABLE in 1 BOTTLE, PLASTIC (70934-140-40) | 2020-03-23 | 0000-00-00 | No | No | Current |