Dicyclomine Hydrochloride
- Product NDC
- 49999-081
- 11-digit product format
- 499990081
- Labeler code
- 49999
- Product ID
- 49999-081_e7468956-701c-41b5-8f97-5be67f7fbb93
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Dicyclomine Hydrochloride
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Lake Erie Medical DBA Quality Care Products LLC
- Application
- ANDA085223
- Marketing category
- ANDA
- Marketing start
- 2011-11-18
- Marketing end
- 0000-00-00
- Substance
- DICYCLOMINE HYDROCHLORIDE
- Active strength
- 20 mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2020-12-31
- 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 |
|---|
| 49999-081-30 | 49999008130 | 30 TABLET in 1 BOTTLE (49999-081-30) | 30 tablet | 2011-11-18 | 0000-00-00 | No | No | Current |
| 49999-081-60 | 49999008160 | 60 TABLET in 1 BOTTLE (49999-081-60) | 60 tablet | 2011-11-18 | 0000-00-00 | No | No | Current |
| 49999-081-90 | 49999008190 | 90 TABLET in 1 BOTTLE (49999-081-90) | 90 tablet | 2011-11-18 | 0000-00-00 | No | No | Current |