Dicyclomine
- Product NDC
- 67296-1741
- 11-digit product format
- 672961741
- Labeler code
- 67296
- Product ID
- 67296-1741_d61f6438-c067-ed1f-e053-2995a90a5ff6
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA040161
- Marketing category
- ANDA
- Marketing start
- 2020-01-01
- 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 Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 67296-1741-1 | Dicyclomine | 10 in 1 BOTTLE | TABLET | 10 | | 8 |
| 67296-1741-7 | Dicyclomine | 15 in 1 BOTTLE | TABLET | 15 | | 8 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 67296-1741 | DICYCLOMINE (DICYCLOMINE HYDROCHLORIDE) TABLET [REDPHARM DRUG, INC.] | 8 | Legacy NDC, 2 package rows | 20240805_a330a08e-0cb6-bc66-e053-2995a90ad9e9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 67296-1741-1 | 67296174101 | 10 TABLET in 1 BOTTLE (67296-1741-1) | 10 tablet | 2020-01-01 | 0000-00-00 | No | No | Current |
| 67296-1741-7 | 67296174107 | 15 TABLET in 1 BOTTLE (67296-1741-7) | 15 tablet | 2020-01-01 | 0000-00-00 | No | No | Current |