Cefadroxil
- Product NDC
- 68180-182
- 11-digit product format
- 681800182
- Labeler code
- 68180
- Product ID
- 68180-182_3818bd15-cf3a-4b07-bef5-57169a33a170
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefadroxil
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA065396
- Marketing category
- ANDA
- Marketing start
- 2008-04-23
- Substance
- CEFADROXIL
- Active strength
- 500 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC], Cephalosporins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Cefadroxil
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CEFADROXIL | 500 mg/5mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 280111G160 |
| Rxcui | 105171, 309048 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68180-182-01 | Cefadroxil | 50 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 50 | | 9 |
| 68180-182-02 | Cefadroxil | 75 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 75 | | 9 |
| 68180-182-03 | Cefadroxil | 100 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 100 | | 9 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| CEFADROXIL | ACTIVE INGREDIENT | 280111G160 | CEFADROXIL POWDER, FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| CEFADROXIL ANHYDROUS | ACTIVE MOIETY | Q525PA8JJB | CEFADROXIL POWDER, FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | CEFADROXIL POWDER, FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| ORANGE | INACTIVE INGREDIENT | 5EVU04N5QU | CEFADROXIL POWDER, FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| PINEAPPLE | INACTIVE INGREDIENT | 2A88ZO081O | CEFADROXIL POWDER, FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | CEFADROXIL POWDER, FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| SODIUM BENZOATE | INACTIVE INGREDIENT | OJ245FE5EU | CEFADROXIL POWDER, FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| SUCROSE | INACTIVE INGREDIENT | C151H8M554 | CEFADROXIL POWDER, FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.] | 3 | |
| XANTHAN GUM | INACTIVE INGREDIENT | TTV12P4NEE | CEFADROXIL POWDER, FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 68180-182 | CEFADROXIL POWDER, FOR SUSPENSION [LUPIN PHARMACEUTICALS, INC.] | 8 | Current NDC, Legacy NDC, 3 package rows | 20250130_27009a05-4d2b-4618-be76-39f348240eda.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68180-182-01 | 68180018201 | 50 mL in 1 BOTTLE (68180-182-01) | 50 ml | 2008-04-23 | 0000-00-00 | No | No | Current |
| 68180-182-02 | 68180018202 | 75 mL in 1 BOTTLE (68180-182-02) | 75 ml | 2008-04-23 | 0000-00-00 | No | No | Current |
| 68180-182-03 | 68180018203 | 100 mL in 1 BOTTLE (68180-182-03) | 100 ml | 2008-04-23 | 0000-00-00 | No | No | Current |