Dicyclomine hydrochloride
- Product NDC
- 68071-5200
- 11-digit product format
- 680715200
- Labeler code
- 68071
- Product ID
- 68071-5200_d773454e-9a56-5ee0-e053-2995a90a1dd7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals,Inc.
- 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
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 |
|---|
| 68071-5200-3 | 68071520003 | 30 CAPSULE in 1 BOTTLE, PLASTIC (68071-5200-3) | 30 capsule | 2020-03-11 | 0000-00-00 | No | No | Current |