Amoxicillin
- Product NDC
- 70518-2333
- 11-digit product format
- 705182333
- Labeler code
- 70518
- Product ID
- 70518-2333_4a02c696-4b58-6767-e063-6394a90ad645
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Amoxicillin
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA065256
- Marketing category
- ANDA
- Marketing start
- 2019-10-01
- Substance
- AMOXICILLIN
- Active strength
- 875 mg/1
- Pharmacologic classes
- Penicillin-class Antibacterial [EPC], Penicillins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Amoxicillin
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| AMOXICILLIN | 875 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 804826J2HU |
| Rxcui | 308194 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-2333-0 | Amoxicillin | 14 in 1 BOTTLE, PLASTIC | TABLET, FILM COATED | 14 | | 7 |
| 70518-2333-1 | Amoxicillin | 20 in 1 BLISTER PACK | TABLET, FILM COATED | 20 | | 7 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2333-0 | 70518233300 | 14 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2333-0) | 2019-10-01 | 0000-00-00 | No | No | Current |
| 70518-2333-1 | 70518233301 | 20 TABLET, FILM COATED in 1 BLISTER PACK (70518-2333-1) | 2019-11-20 | 0000-00-00 | No | No | Current |