Cefepime
- Product NDC
- 60505-6146
- 11-digit product format
- 605056146
- Labeler code
- 60505
- Product ID
- 60505-6146_e1dbb0ac-a9df-41c4-acb2-3e3f5732f7ef
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Cefepime
- Dosage form
- INJECTION, POWDER, FOR SOLUTION
- Route
- INTRAMUSCULAR; INTRAVENOUS
- Labeler
- Apotex Corp.
- Application
- ANDA203704
- Marketing category
- ANDA
- Marketing start
- 2017-03-30
- Substance
- CEFEPIME HYDROCHLORIDE
- Active strength
- 1 g/1
- 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
- Cefepime
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| CEFEPIME HYDROCHLORIDE | 1 g/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | I8X1O0607P |
| Rxcui | 1665088, 1665093 |
DailyMed Product Concepts#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 60505-6146 | CEFEPIME INJECTION, POWDER, FOR SOLUTION [APOTEX CORP.] | 10 | Current NDC, Legacy NDC | 20230512_dd641c7f-b857-48ff-bd9d-747e0c3cc89f.zip |
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 |
|---|
| 60505-6146-0 | 60505614600 | 1 VIAL, SINGLE-DOSE in 1 CARTON (60505-6146-0) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE | 2017-03-30 | 0000-00-00 | No | No | Current |
| 60505-6146-4 | 60505614604 | 10 VIAL, SINGLE-DOSE in 1 CARTON (60505-6146-4) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE | 2017-03-30 | 0000-00-00 | No | No | Current |