Dicyclomine
- Product NDC
- 70934-518
- 11-digit product format
- 709340518
- Labeler code
- 70934
- Product ID
- 70934-518_a93f355e-7c37-84d5-e053-2995a90a0b67
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA040161
- Marketing category
- ANDA
- Marketing start
- 2020-01-28
- Marketing end
- 0000-00-00
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 70934-518-20 | 70934051820 | 20 TABLET in 1 BOTTLE, PLASTIC (70934-518-20) | 20 tablet | 2020-01-28 | 0000-00-00 | No | No | Current |
| 70934-518-30 | 70934051830 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-518-30) | 30 tablet | 2020-02-12 | 0000-00-00 | No | No | Current |