Dicyclomine Hydrochloride
- Product NDC
- 70518-3220
- 11-digit product format
- 705183220
- Labeler code
- 70518
- Product ID
- 70518-3220_cbe6d19c-a68f-e9cf-e053-2a95a90a8d0d
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA212286
- Marketing category
- ANDA
- Marketing start
- 2021-09-13
- Marketing end
- 0000-00-00
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 10 mg/5mL
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- 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 |
|---|
| 70518-3220-0 | 70518322000 | 473 mL in 1 BOTTLE (70518-3220-0) | 473 ml | 2021-09-13 | 0000-00-00 | No | No | Current |