ALBOTHYL
- Product NDC
- 72689-0040
- 11-digit product format
- 726890040
- Labeler code
- 72689
- Product ID
- 72689-0040_847dd36e-0865-6ce1-e053-2a91aa0a82cf
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Policresulen Solution
- Dosage form
- SOLUTION
- Route
- BUCCAL; VAGINAL
- Labeler
- OASIS TRADING
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-11-21
- Marketing end
- 0000-00-00
- Substance
- POLICRESULEN
- Active strength
- 720 mg/mL
- 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 |
|---|
| 72689-0040-1 | ALBOTHYL | 5 mL in 1 BOTTLE | SOLUTION | 5 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72689-0040 | ALBOTHYL (POLICRESULEN SOLUTION) SOLUTION [OASIS TRADING] | 1 | Legacy NDC, 1 package rows | 20190320_847dca04-cfe6-19be-e053-2991aa0a04df.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 72689-0040-1 | 72689004001 | 5 mL in 1 BOTTLE | 5 ml | Historical |