Cephalexin
- Product NDC
- 59834-202
- 11-digit product format
- 598340202
- Labeler code
- 59834
- Product ID
- 59834-202_d44b632d-0f53-4063-9479-27b5f9a92727
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cephalexin
- Dosage form
- POWDER, FOR SUSPENSION
- Route
- ORAL
- Labeler
- OrchidPharma Inc
- Application
- ANDA065326
- Marketing category
- ANDA
- Marketing start
- 2011-09-01
- Marketing end
- 0000-00-00
- Substance
- CEPHALEXIN
- Active strength
- 125 mg/5mL
- Pharmacologic classes
- Cephalosporin Antibacterial [EPC],Cephalosporins [CS]
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
| Product concept | Relation | Version | Effective |
|---|---|---|---|
| dfa3f520-409c-432e-b6d3-9250d468c772 | Product name | 1 | 20250401 |
| 64bb7f1a-2c2e-4741-8301-dbfeda7239f6 | Product name | 1 | 20190628 |
| 398aa563-bb78-fe0f-46a8-757c40ef28bf | Product name | 1 | 20140508 |
FDA-Initiated Inactive NDC Indexing#
| NDC | Effective | Action | Document | Indexing SPL | Related label |
|---|---|---|---|---|---|
| 59834-202-17 | 2019-11-13 | C162847 | 48780-1 | 97449f38-bae3-f6ea-e053-dbdaa90aa703 | CEPHALEXIN FOR ORAL SUSPENSION, USP Rx only |
| 59834-202-47 | 2019-11-13 | C162847 | 48780-1 | 97449f38-bae3-f6ea-e053-dbdaa90aa703 | CEPHALEXIN FOR ORAL SUSPENSION, USP Rx only |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 59834-202-17 | Cephalexin | 100 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 100 | 2 | |
| 59834-202-47 | Cephalexin | 200 mL in 1 BOTTLE | POWDER, FOR SUSPENSION | 200 | 2 |
DailyMed Socrata Ingredients#
| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|---|---|---|---|---|
| CEPHALEXIN | ACTIVE INGREDIENT | OBN7UDS42Y | CEPHALEXIN POWDER, FOR SUSPENSION [ORCHIDPHARMA INC] | 2 | |
| CEPHALEXIN ANHYDROUS | ACTIVE MOIETY | 5SFF1W6677 | CEPHALEXIN POWDER, FOR SUSPENSION [ORCHIDPHARMA INC] | 2 | |
| FD&C YELLOW NO. 6 | INACTIVE INGREDIENT | H77VEI93A8 | CEPHALEXIN POWDER, FOR SUSPENSION [ORCHIDPHARMA INC] | 2 | |
| SILICON DIOXIDE | INACTIVE INGREDIENT | ETJ7Z6XBU4 | CEPHALEXIN POWDER, FOR SUSPENSION [ORCHIDPHARMA INC] | 2 | |
| SODIUM LAURYL SULFATE | INACTIVE INGREDIENT | 368GB5141J | CEPHALEXIN POWDER, FOR SUSPENSION [ORCHIDPHARMA INC] | 2 | |
| SUCROSE | INACTIVE INGREDIENT | C151H8M554 | CEPHALEXIN POWDER, FOR SUSPENSION [ORCHIDPHARMA INC] | 2 | |
| XANTHAN GUM | INACTIVE INGREDIENT | TTV12P4NEE | CEPHALEXIN POWDER, FOR SUSPENSION [ORCHIDPHARMA INC] | 2 |
DailyMed Dashboard NDC Coverage#
DailyMed RxNorm Mappings#
| RxCUI | RxNorm string | TTY | DailyMed | SPL version |
|---|---|---|---|---|
| 309110 | cephalexin 125 MG in 5 mL Oral Suspension | PSN | cb31cd1b-100d-4a24-b314-1ddcd6a95314 | 2 |
| 309113 | cephalexin 250 MG in 5 mL Oral Suspension | PSN | cb31cd1b-100d-4a24-b314-1ddcd6a95314 | 2 |
| 309110 | cephalexin 25 MG/ML Oral Suspension | SCD | cb31cd1b-100d-4a24-b314-1ddcd6a95314 | 2 |
| 309113 | cephalexin 50 MG/ML Oral Suspension | SCD | cb31cd1b-100d-4a24-b314-1ddcd6a95314 | 2 |
| 309110 | cefalexin 25 MG/ML Oral Suspension | SY | cb31cd1b-100d-4a24-b314-1ddcd6a95314 | 2 |
| 309113 | cefalexin 50 MG/ML Oral Suspension | SY | cb31cd1b-100d-4a24-b314-1ddcd6a95314 | 2 |
| 309110 | cephalexin 125 MG per 5 ML Oral Suspension | SY | cb31cd1b-100d-4a24-b314-1ddcd6a95314 | 2 |
| 309113 | cephalexin 250 MG per 5 ML Oral Suspension | SY | cb31cd1b-100d-4a24-b314-1ddcd6a95314 | 2 |
Packages#
| Package NDC | 11-digit format | Description | Units | Status |
|---|---|---|---|---|
| 59834-202-17 | 59834020217 | 100 mL in 1 BOTTLE | 100 ml | Historical |
| 59834-202-47 | 59834020247 | 200 mL in 1 BOTTLE | 200 ml | Historical |