Amoxicillin
- Product NDC
- 72508-225
- 11-digit product format
- 725080225
- Labeler code
- 72508
- Product ID
- 72508-225_f662c7f8-9515-4706-9cc9-5079956b6365
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Neopharma Inc
- Application
- ANDA062216
- Marketing category
- ANDA
- Marketing start
- 2019-04-03
- Marketing end
- 2022-11-01
- Substance
- AMOXICILLIN
- Active strength
- 250 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC],Penicillins [CS]
- 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 |
|---|
| 72508-225-01 | 72508022501 | 100 CAPSULE in 1 BOTTLE (72508-225-01) | 100 capsule | 2019-04-03 | 0000-00-00 | No | No | Current |
| 72508-225-05 | 72508022505 | 500 CAPSULE in 1 BOTTLE (72508-225-05) | 500 capsule | 2019-04-03 | 0000-00-00 | No | No | Current |