Dicyclomine Hydrochloride
- Product NDC
- 67296-1304
- 11-digit product format
- 672961304
- Labeler code
- 67296
- Product ID
- 67296-1304_9c9f47ba-7769-719e-e053-2995a90adffe
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- RedPharm Drug, Inc.
- Application
- ANDA040317
- Marketing category
- ANDA
- Marketing start
- 1999-11-03
- 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 |
|---|---|---|---|---|---|---|---|---|
| 67296-1304-1 | 67296130401 | 10 TABLET in 1 BOTTLE (67296-1304-1) | 10 tablet | 1999-11-03 | 0000-00-00 | No | No | Current |
| 67296-1304-5 | 67296130405 | 56 TABLET in 1 BOTTLE (67296-1304-5) | 56 tablet | 1999-11-03 | 0000-00-00 | No | No | Current |