FUCIDIN
- Product NDC
- 72689-0006
- 11-digit product format
- 726890006
- Labeler code
- 72689
- Product ID
- 72689-0006_7b220787-cf10-6f50-e053-2a91aa0aab6e
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fusidate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- OASIS TRADING
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-11-21
- Marketing end
- 0000-00-00
- Substance
- FUSIDATE SODIUM
- Active strength
- 20 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2019-12-31
- 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 |
|---|
| 72689-0006-1 | FUCIDIN | 10 g in 1 TUBE | OINTMENT | 10 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72689-0006 | FUCIDIN (SODIUM FUSIDATE) OINTMENT [OASIS TRADING] | 1 | Legacy NDC, 1 package rows | 20181121_7b220787-cf0f-6f50-e053-2a91aa0aab6e.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 72689-0006-1 | 72689000601 | 10 g in 1 TUBE | 10 g | Historical |