Dicyclomine Hydrochloride
- Product NDC
- 70934-182
- 11-digit product format
- 709340182
- Labeler code
- 70934
- Product ID
- 70934-182_d4643219-31cf-742f-e053-2a95a90a7693
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals
- Application
- ANDA040230
- Marketing category
- ANDA
- Marketing start
- 2019-12-05
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70934-182-30 | 70934018230 | 30 TABLET in 1 BOTTLE, PLASTIC (70934-182-30) | 30 tablet | 2018-10-29 | 0000-00-00 | No | No | Current |