Dicyclomine Hydrochloride 16571-0259
Product NDC
16571-0259- Manufacturer
- Rising Pharma Holdings, Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- November 15, 2024
- Listing Expires
- December 31, 2027
- Application
- ANDA218952
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Dicyclomine Hydrochloride | 20 mg/1 |
Drug Class
Anticholinergic [EPC]Cholinergic Antagonists [MoA]
Packaging Options(2)
100 TABLET in 1 BOTTLE (16571-259-01)
1000 TABLET in 1 BOTTLE (16571-259-10)