ALBOTHYL
- Product NDC
- 72988-0035
- 11-digit product format
- 729880035
- Labeler code
- 72988
- Product ID
- 72988-0035_001d54ef-148b-e55a-e063-6294a90a7c40
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Policresulen Solution
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Lydia Co., Ltd.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2023-01-23
- Substance
- POLICRESULEN
- Active strength
- 720 mg/g
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- ALBOTHYL
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| POLICRESULEN | 720 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 6I19M5GB0G |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72988-0035-1 | ALBOTHYL | 5 g in 1 BOTTLE | LIQUID | 5 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72988-0035 | ALBOTHYL (POLICRESULEN SOLUTION) LIQUID [LYDIA CO., LTD.] | 3 | Current NDC, 1 package rows | 20230819_f2ea4e1b-a3d7-d063-e053-2a95a90a6d0b.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72988-0035-1 | 72988003501 | 5 g in 1 BOTTLE (72988-0035-1) | 5 g | 2023-01-23 | No | No | Current |