Amoxicillin and Clavulanate Potassium
- Product NDC
- 72508-221
- 11-digit product format
- 725080221
- Labeler code
- 72508
- Product ID
- 72508-221_5389440b-425b-4a38-896e-b47005af3f45
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin and Clavulanate Potassium
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Neopharma Inc
- Application
- NDA050720
- Marketing category
- NDA
- Marketing start
- 2019-12-12
- Marketing end
- 2022-06-01
- Substance
- AMOXICILLIN; CLAVULANATE POTASSIUM
- Active strength
- 875 mg/1; mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS],beta Lactamase Inhibitor [EPC],beta Lactamase Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 72508-221-14 | 72508022114 | 20 TABLET in 1 BOTTLE (72508-221-14) | 20 tablet | 2019-12-12 | 0000-00-00 | No | No | Current |
| 72508-221-78 | 72508022178 | 100 TABLET in 1 BOX, UNIT-DOSE (72508-221-78) | 100 tablet | 2019-12-12 | 0000-00-00 | No | No | Current |