VRMX 500
- Product NDC
- 69729-141
- 11-digit product format
- 697290141
- Labeler code
- 69729
- Product ID
- 69729-141_10c1a1dd-9165-2eec-e063-6294a90a3a38
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- PYRANTEL PAMOATE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- OPMX LLC
- Application
- M024
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-06-10
- Substance
- PYRANTEL PAMOATE
- Active strength
- 180 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- VRMX 500
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| PYRANTEL PAMOATE | 180 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 81BK194Z5M |
| Rxcui | 199107 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 69729-141-10 | VRMX 500 | 10 in 1 BLISTER PACK | TABLET | 10 | | 6 |
| 69729-141-10 | VRMX 500 | 1 in 1 CARTON | TABLET | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 69729-141 | VRMX 500 (PYRANTEL PAMOATE) TABLET [OPMX LLC] | 6 | Current NDC, Legacy NDC, 2 package rows | 20240209_e119cad8-9814-7d5a-e053-2995a90afde5.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 69729-141-10 | 69729014110 | 1 BLISTER PACK in 1 CARTON (69729-141-10) / 10 TABLET in 1 BLISTER PACK | 1 blister pack | 2022-06-10 | 0000-00-00 | No | No | Current |