FUCIDIN
- Product NDC
- 73442-0001
- 11-digit product format
- 734420001
- Labeler code
- 73442
- Product ID
- 73442-0001_96b7b864-2571-8570-e053-2995a90a176b
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Sodium Fusidate
- Dosage form
- OINTMENT
- Route
- TOPICAL
- Labeler
- I World Pharmaceutical 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 Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 73442-0001 | FUCIDIN (SODIUM FUSIDATE) OINTMENT [I WORLD PHARMACEUTICAL CO., LTD.] | 2 | Legacy NDC | 20250215_96b7b841-0954-85a2-e053-2995a90aafdf.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 73442-0001-1 | 73442000101 | 10 g in 1 TUBE (73442-0001-1) | 10 g | 2019-10-08 | 0000-00-00 | No | No | Current |