FUCIDIN
- Product NDC
- 72988-0015
- 11-digit product format
- 729880015
- Labeler code
- 72988
- Product ID
- 72988-0015_94587991-bc94-fcfd-e053-2995a90af86a
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fusidate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- Lydia Co., Ltd.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-10-08
- Marketing end
- 0000-00-00
- Substance
- FUSIDATE SODIUM
- Active strength
- 20 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 72988-0015-1 | 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 |
|---|
| 72988-0015 | FUCIDIN (SODIUM FUSIDATE) OINTMENT [LYDIA CO., LTD.] | 1 | Legacy NDC, 1 package rows | 20191008_94586c4c-da34-47e0-e053-2a95a90a144c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 72988-0015-1 | 72988001501 | 10 g in 1 TUBE | 10 g | Historical |