Dicyclomine hydrochloride
- Product NDC
- 0904-6969
- 11-digit product format
- 009046969
- Labeler code
- 0904
- Product ID
- 0904-6969_af3953df-0f97-4723-9e5b-8037600f7faa
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- 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
- 2023-12-31
- 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 |
|---|
| 0904-6969-60 | 00904696960 | 100 CAPSULE in 1 BOTTLE, PLASTIC (0904-6969-60) | 100 capsule | 1997-02-28 | 2021-05-31 | No | No | Current |
| 0904-6969-80 | 00904696980 | 1000 CAPSULE in 1 BOTTLE, PLASTIC (0904-6969-80) | 1000 capsule | 1997-02-28 | 0000-00-00 | No | No | Current |