Amoxicillin
- Product NDC
- 50090-1796
- 11-digit product format
- 500901796
- Labeler code
- 50090
- Product ID
- 50090-1796_54c09f75-0b96-460c-9c9b-ad35e8c1fd15
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- A-S Medication Solutions
- Application
- ANDA065271
- Marketing category
- ANDA
- Marketing start
- 2005-11-09
- Substance
- AMOXICILLIN
- Active strength
- 500 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 804826J2HU | AMOXICILLIN | 61336-70-7 | AMOXICILLIN |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 50090-1796-0 | 50090179600 | 14 CAPSULE in 1 BOTTLE (50090-1796-0) | 14 capsule | 2015-04-29 | No | No | Historical |
| 50090-1796-1 | 50090179601 | 60 CAPSULE in 1 BOTTLE (50090-1796-1) | 60 capsule | 2020-04-09 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | A-S Medication Solutions | 2024-11-04 | Human Prescription Drug Label | 8 |