Amoxicillin
- Product NDC
- 50090-4929
- 11-digit product format
- 500904929
- Labeler code
- 50090
- Product ID
- 50090-4929_060e6644-bc5d-4dc3-94d1-b6e3f5d41746
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065056
- Marketing category
- ANDA
- Marketing start
- 2000-09-26
- 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
- 2021-12-31
- 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 | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-4929-0 | 50090492900 | 20 TABLET, FILM COATED in 1 BOTTLE (50090-4929-0) | 2020-02-24 | 0000-00-00 | No | No | Current |
| 50090-4929-1 | 50090492901 | 14 TABLET, FILM COATED in 1 BOTTLE (50090-4929-1) | 2020-02-24 | 0000-00-00 | No | No | Current |
| 50090-4929-2 | 50090492902 | 30 TABLET, FILM COATED in 1 BOTTLE (50090-4929-2) | 2020-02-24 | 0000-00-00 | No | No | Current |