Dicyclomine hydrochloride
- Product NDC
- 68071-3885
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA217566
- Marketing category
- ANDA
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 68071-3885-2 | 20 TABLET in 1 BOTTLE (68071-3885-2) | 2025-08-15 | | No | Historical |
| 68071-3885-3 | 30 TABLET in 1 BOTTLE (68071-3885-3) | 2025-08-15 | | No | Historical |
| 68071-3885-6 | 60 TABLET in 1 BOTTLE (68071-3885-6) | 2025-11-03 | | No | Historical |