Dicyclomine Hydrochloride
- Product NDC
- 68788-9291
- 11-digit product format
- 687889291
- Labeler code
- 68788
- Product ID
- 68788-9291_183ebbfd-3d68-4d4e-bb63-44ecb69653c3
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dicyclomine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA040317
- Marketing category
- ANDA
- Marketing start
- 2015-05-13
- 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 |
|---|
| 68788-9291-1 | 68788929101 | 100 TABLET in 1 BOTTLE, PLASTIC (68788-9291-1) | 100 tablet | 2015-05-13 | 0000-00-00 | No | No | Current |
| 68788-9291-2 | 68788929102 | 20 TABLET in 1 BOTTLE, PLASTIC (68788-9291-2) | 20 tablet | 2015-05-13 | 0000-00-00 | No | No | Current |
| 68788-9291-3 | 68788929103 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-9291-3) | 30 tablet | 2015-05-13 | 0000-00-00 | No | No | Current |
| 68788-9291-6 | 68788929106 | 60 TABLET in 1 BOTTLE, PLASTIC (68788-9291-6) | 60 tablet | 2015-05-13 | 0000-00-00 | No | No | Current |