Dicyclomine Hydrochloride
- Product NDC
- 60760-931
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA216782
- Marketing category
- ANDA
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 60760-931-30 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-931-30) | 2024-12-30 | | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Dicyclomine Hydrochloride | ST. MARY'S MEDICAL PARK PHARMACY | 2025-01-03 | HUMAN PRESCRIPTION DRUG LABEL | 1 |