Kondremul
- Product NDC
- 63736-012
- 11-digit product format
- 637360012
- Labeler code
- 63736
- Product ID
- 63736-012_856ae077-f23b-40bf-9a06-09e6f0d56d19
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Kondremul
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Insight Pharmaceuticals
- Application
- part334
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2009-06-05
- Marketing end
- 0000-00-00
- Substance
- MINERAL OIL
- Active strength
- 3 mL/5mL
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 63736-012-16 | Kondremul | 480 mL in 1 BOTTLE | LIQUID | 480 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63736-012 | KONDREMUL LIQUID [INSIGHT PHARMACEUTICALS] | 2 | Legacy NDC, 1 package rows | 20100302_116e0ea5-c649-47ef-a9d2-fc683aed229c.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Status |
|---|
| 63736-012-16 | 63736001216 | 480 mL in 1 BOTTLE | 480 ml | Historical |