Dicyclomine Hydrochloride
- Product NDC
- 63629-6320
- 11-digit product format
- 636296320
- Labeler code
- 63629
- Product ID
- 63629-6320_eb47a73e-0395-4243-851e-b0c0304e5902
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- dicyclomine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA040319
- Marketing category
- ANDA
- Marketing start
- 1999-11-03
- Marketing end
- 0000-00-00
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 10 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
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 |
|---|
| 63629-6320-1 | 63629632001 | 90 CAPSULE in 1 BOTTLE (63629-6320-1) | 90 capsule | 2015-09-04 | 0000-00-00 | No | No | Current |
| 63629-6320-2 | 63629632002 | 30 CAPSULE in 1 BOTTLE (63629-6320-2) | 30 capsule | 2015-09-04 | 0000-00-00 | No | No | Current |