Dicyclomine Hydrochloride
- Product NDC
- 70518-0327
- 11-digit product format
- 705180327
- Labeler code
- 70518
- Product ID
- 70518-0327_ea3724d7-947b-c835-e053-2a95a90a4ac2
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA084285
- Marketing category
- ANDA
- Marketing start
- 2017-03-17
- 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 |
|---|
| 70518-0327-0 | 70518032700 | 30 CAPSULE in 1 BLISTER PACK (70518-0327-0) | 30 capsule | 2017-03-17 | 0000-00-00 | No | No | Current |