Mebrofenin
- Product NDC
- 51808-216
- 11-digit product format
- 518080216
- Labeler code
- 51808
- Product ID
- 51808-216_4d7406b4-8bcd-40f0-a31f-975f5b811da7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Mebrofenin
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- AnazaoHealth Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2012-06-19
- Marketing end
- 0000-00-00
- Substance
- MEBROFENIN
- Active strength
- 10 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 51808-216-01 | Mebrofenin | 1 in 1 KIT | INJECTION, POWDER, LYOPHILIZED, | 1 | | 3 |
DailyMed Socrata Ingredients#
Ingredient, Type, UNII table| Ingredient | Type | UNII | DailyMed label | SPL version | Uploaded |
|---|
| MEBROFENIN | ACTIVE INGREDIENT | 7PV0B6ED98 | MEBROFENIN INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ANAZAOHEALTH CORPORATION] | 3 | |
| MEBROFENIN | ACTIVE MOIETY | 7PV0B6ED98 | MEBROFENIN INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ANAZAOHEALTH CORPORATION] | 3 | |
| STANNOUS CHLORIDE | INACTIVE INGREDIENT | 1BQV3749L5 | MEBROFENIN INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ANAZAOHEALTH CORPORATION] | 3 | |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 51808-216 | MEBROFENIN INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [ANAZAOHEALTH CORPORATION] | 3 | Legacy NDC, 1 package rows | 20120726_aeefa6ee-f45c-49fe-b38e-6cfd99a33030.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 51808-216-01 | 51808021601 | 1 in 1 KIT | Historical |