Amoxicillin
- Product NDC
- 63629-7584
- 11-digit product format
- 636297584
- Labeler code
- 63629
- Product ID
- 63629-7584_41d91cb9-8582-dc65-e063-6394a90a22a5
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- 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
openFDA Listing Details
- Product ID
- 63629-7584_41d91cb9-8582-dc65-e063-6394a90a22a5
- Product type
- HUMAN PRESCRIPTION DRUG
- Finished product
- Yes
- Brand name base
- Amoxicillin
- Generic name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Marketing start
- 2005-11-09
- Marketing category
- ANDA
- Application number
- ANDA065271
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC]; Penicillins [CS]
- Listing expiration
- 2026-12-31
openFDA Active Ingredients
| Ingredient | Strength |
|---|
| AMOXICILLIN | 500 mg/1 |
openFDA Harmonized Identifiers
| Field | Values |
|---|
| Unii | 804826J2HU |
| Rxcui | 308191 |
| Spl Set Id | bbaeb509-ad04-4668-a1db-4358038893f2 |
| Manufacturer Name | Bryant Ranch Prepack |
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-7584-1 | 63629758401 | 30 CAPSULE in 1 BOTTLE (63629-7584-1) | 30 capsule | 2005-11-09 | 0000-00-00 | No | No | Current |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Amoxicillin | Bryant Ranch Prepack | 2025-10-23 | HUMAN PRESCRIPTION DRUG LABEL | 3 |