Dicyclomine hydrochloride
- Product NDC
- 51407-365
- 11-digit product format
- 514070365
- Labeler code
- 51407
- Product ID
- 51407-365_a837a5a3-865d-4377-e053-2995a90a59c1
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Golden State Medical Supply
- Application
- ANDA040204
- Marketing category
- ANDA
- Marketing start
- 1997-02-28
- 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
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 51407-365-01 | 51407036501 | 100 CAPSULE in 1 BOTTLE, PLASTIC (51407-365-01) | 100 capsule | 2020-03-12 | 0000-00-00 | No | No | Current |
| 51407-365-10 | 51407036510 | 1000 CAPSULE in 1 BOTTLE, PLASTIC (51407-365-10) | 1000 capsule | 2020-03-12 | 0000-00-00 | No | No | Current |