Hyoscyamine Sulfate
- Product NDC
- 72162-1939
- 11-digit product format
- 721621939
- Labeler code
- 72162
- Product ID
- 72162-1939_51e502c9-5761-4bdf-933b-372169555e69
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Hyoscyamine Sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2018-10-01
- Substance
- HYOSCYAMINE SULFATE
- Active strength
- .125 mg/1
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| F2R8V82B84 | HYOSCYAMINE SULFATE | 6835-16-1 | HYOSCYAMINE SULFATE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1939-1 | 72162193901 | 100 TABLET in 1 BOTTLE (72162-1939-1) | 100 tablet | 2023-08-31 | No | No | Historical |