Dicyclomine hydrochloride
- Product NDC
- 60760-802
- 11-digit product format
- 607600802
- Labeler code
- 60760
- Product ID
- 60760-802_41aecc7f-7307-438a-e063-6294a90a85bb
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- ST. MARY'S MEDICAL PARK PHARMACY
- Application
- ANDA216736
- Marketing category
- ANDA
- Marketing start
- 2022-12-14
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Anticholinergic [EPC], Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| CQ903KQA31 | DICYCLOMINE HYDROCHLORIDE | 67-92-5 | DICYCLOMINE HYDROCHLORIDE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 60760-802-30 | 60760080230 | 30 TABLET in 1 BOTTLE, PLASTIC (60760-802-30) | 30 tablet | 2025-10-21 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Dicyclomine hydrochloride | ST. MARY'S MEDICAL PARK PHARMACY | 2025-10-21 | HUMAN PRESCRIPTION DRUG LABEL | 1 |