Digenyx
- Product NDC
- 59088-150
- 11-digit product format
- 590880150
- Labeler code
- 59088
- Product ID
- 59088-150_512f3202-4ed0-1218-e063-6294a90a0544
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hyoscyamine Sulfate 0.125 mg
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- PureTek Corporation
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-05-13
- Substance
- HYOSCYAMINE SULFATE
- Active strength
- .125 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Digenyx
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| HYOSCYAMINE SULFATE | .125 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | F2R8V82B84 |
| Rxcui | 1047905, 2743192 |
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59088-150-54 | Digenyx | 30 in 1 BOTTLE | TABLET | 30 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 59088-150-54 | 59088015054 | 30 TABLET in 1 BOTTLE (59088-150-54) | 30 tablet | 2026-05-13 | No | No | Current |