Hyoscyamine Sulfate
- Product NDC
- 21695-442
- 11-digit product format
- 216950442
- Labeler code
- 21695
- Product ID
- 21695-442_44c85649-a82e-4c1e-bf3d-b168296d8d0e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hyoscyamine Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Rebel Distributors Corp
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2009-11-05
- Marketing end
- 0000-00-00
- Substance
- HYOSCYAMINE SULFATE
- Active strength
- 0 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 |
|---|
| 21695-442-10 | Hyoscyamine Sulfate | 10 in 1 BOTTLE | TABLET | 10 | | 2 |
| 21695-442-20 | Hyoscyamine Sulfate | 20 in 1 BOTTLE | TABLET | 20 | | 2 |
DailyMed Socrata Ingredients#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 21695-442 | HYOSCYAMINE SULFATE TABLET [REBEL DISTRIBUTORS CORP] | 2 | Legacy NDC, 2 package rows | 20111021_e219b697-45d8-4388-8c79-4b98961fc525.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Status |
|---|
| 21695-442-10 | 21695044210 | 10 in 1 BOTTLE | Historical |
| 21695-442-20 | 21695044220 | 20 in 1 BOTTLE | Historical |