Dicyclomine Hydrochloride
- Product NDC
- 72162-1077
- 11-digit product format
- 721621077
- Labeler code
- 72162
- Product ID
- 72162-1077_5912cfd5-c3e7-41e0-93cd-f051f6446e3f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040230
- Marketing category
- ANDA
- Marketing start
- 1999-02-26
- 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 |
|---|
| 72162-1077-3 | 72162107703 | 30 TABLET in 1 BOTTLE (72162-1077-3) | 30 tablet | 2023-05-08 | No | No | Historical |
| 72162-1077-9 | 72162107709 | 90 TABLET in 1 BOTTLE (72162-1077-9) | 90 tablet | 2023-05-08 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| Dicyclomine Hydrochloride | Bryant Ranch Prepack | 2023-05-08 | HUMAN PRESCRIPTION DRUG LABEL | 100 |