Dicyclomine Hydrochloride
- Product NDC
- 70518-2081
- 11-digit product format
- 705182081
- Labeler code
- 70518
- Product ID
- 70518-2081_c5ea7475-0a57-5630-e053-2995a90a125f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA085082
- Marketing category
- ANDA
- Marketing start
- 2019-05-14
- Marketing end
- 0000-00-00
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 10 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
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 | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-2081-0 | 70518208100 | 30 CAPSULE in 1 BLISTER PACK (70518-2081-0) | 30 capsule | 2019-05-14 | 0000-00-00 | No | No | Current |
| 70518-2081-1 | 70518208101 | 100 CAPSULE in 1 BOTTLE, PLASTIC (70518-2081-1) | 100 capsule | 2020-07-31 | 0000-00-00 | No | No | Current |