Hyoscyamine Sulfate
- Product NDC
- 72789-563
- 11-digit product format
- 727890563
- Labeler code
- 72789
- Product ID
- 72789-563_5191a27f-ba08-8d37-e063-6394a90a61f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hyoscyamine Sulfate
- Dosage form
- TABLET, ORALLY DISINTEGRATING
- Route
- ORAL
- Labeler
- PD-Rx Pharmaceuticals, Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2026-04-16
- 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
- Hyoscyamine Sulfate
- 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 | 1046985 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72789-563-01 | Hyoscyamine Sulfate | 100 in 1 BOTTLE, PLASTIC | TABLET, ORALLY DISINTEGRATING | 100 | | 2 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72789-563-01 | 72789056301 | 100 TABLET, ORALLY DISINTEGRATING in 1 BOTTLE, PLASTIC (72789-563-01) | 2026-05-11 | No | No | Historical |