ISOXSUPRINE HYDROCHLORIDE
- Product NDC
- 63549-919
- 11-digit product format
- 635490919
- Labeler code
- 63549
- Product ID
- 63549-919_e6f0f0dd-940a-490f-a404-56dd561264e6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- isoxsuprine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Vedco dba Valdar
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2011-08-23
- Marketing end
- 0000-00-00
- Substance
- ISOXSUPRINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- NDC exclude flag
- E
- Listing certified through
- 2017-12-31
- 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 |
|---|
| 63549-919-53 | ISOXSUPRINE HYDROCHLORIDE | 1000 in 1 BOTTLE, PLASTIC | TABLET | 1000 | | 1 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 63549-919 | ISOXSUPRINE HYDROCHLORIDE TABLET [VEDCO DBA VALDAR] | 1 | Legacy NDC, 1 package rows | 20120207_908691b4-7950-4f3e-bbea-ea568fee7ac3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 63549-919-53 | 63549091953 | 1000 in 1 BOTTLE, PLASTIC | Historical |