Podocon 25
- Product NDC
- 63629-8699
- 11-digit product format
- 636298699
- Labeler code
- 63629
- Product ID
- 63629-8699_01196278-c8ea-4b89-8e71-eed68e8be55a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Podophyllum resin
- Dosage form
- TINCTURE
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 1990-09-01
- Substance
- PODOPHYLLUM RESIN
- Active strength
- 1 mg/4mL
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Podocon 25
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PODOPHYLLUM RESIN | 1 mg/4mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 16902YVY2B |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63629-8699-1 | Podocon 25 | 1 in 1 CARTON | TINCTURE | 1 | | 103 |
| 63629-8699-1 | Podocon 25 | 15 mL in 1 BOTTLE, WITH APPLICATOR | TINCTURE | 15 | | 103 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63629-8699 | PODOCON 25 (PODOPHYLLUM RESIN) TINCTURE [BRYANT RANCH PREPACK] | 103 | Current NDC, Legacy NDC, 2 package rows | 20230718_a13345b7-c42b-4459-b0ff-03cf91e46b7d.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-8699-1 | 63629869901 | 1 BOTTLE, WITH APPLICATOR in 1 CARTON (63629-8699-1) / 15 mL in 1 BOTTLE, WITH APPLICATOR | 1990-09-01 | 0000-00-00 | No | No | Current |