Dicyclomine Hydrochloride
- Product NDC
- 68788-9525
- 11-digit product format
- 687889525
- Labeler code
- 68788
- Product ID
- 68788-9525_9e6a6c26-8cf1-4cac-8ea2-ffee0155536e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Preferred Pharmaceuticals, Inc.
- Application
- ANDA085223
- Marketing category
- ANDA
- Marketing start
- 2014-02-21
- 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
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-9525-2 | 68788952502 | 20 TABLET in 1 BOTTLE, PLASTIC (68788-9525-2) | 20 tablet | 2014-02-21 | 0000-00-00 | No | No | Current |
| 68788-9525-3 | 68788952503 | 30 TABLET in 1 BOTTLE, PLASTIC (68788-9525-3) | 30 tablet | 2014-02-21 | 0000-00-00 | No | No | Current |