Dicyclomine Hydrochloride
- Product NDC
- 70518-0755
- 11-digit product format
- 705180755
- Labeler code
- 70518
- Product ID
- 70518-0755_eed93421-0788-596c-e053-2a95a90a114d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA040230
- Marketing category
- ANDA
- Marketing start
- 2017-10-02
- 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
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-0755 | DICYCLOMINE HYDROCHLORIDE TABLET [REMEDYREPACK INC.] | 10 | Legacy NDC | 20250429_f7c25c58-4432-4bd8-a842-de5104add455.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 70518-0755-1 | 70518075501 | 180 TABLET in 1 BOTTLE, PLASTIC (70518-0755-1) | 180 tablet | 2019-01-30 | 0000-00-00 | No | No | Current |