Amoxicillin
- Product NDC
- 70518-1413
- 11-digit product format
- 705181413
- Labeler code
- 70518
- Product ID
- 70518-1413_e4186c10-5503-4fe3-e053-2995a90a59f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065228
- Marketing category
- ANDA
- Marketing start
- 2018-09-12
- Marketing end
- 0000-00-00
- Substance
- AMOXICILLIN
- Active strength
- 875 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 |
|---|
| 70518-1413-1 | 70518141301 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1413-1) | 2021-09-21 | 0000-00-00 | No | No | Current |