Dicyclomine Hydrochloride
- Product NDC
- 70518-0236
- 11-digit product format
- 705180236
- Labeler code
- 70518
- Product ID
- 70518-0236_bccb6000-f24d-68d6-e053-2995a90a6b69
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dicyclomine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040317
- Marketing category
- ANDA
- Marketing start
- 2017-02-17
- 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
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0236-2 | 70518023602 | 180 TABLET in 1 BOTTLE, PLASTIC (70518-0236-2) | 180 tablet | 2020-01-24 | 0000-00-00 | No | No | Current |