Diphenoxylate Hydrochloride and Atropine Sulfate
- Product NDC
- 66267-082
- 11-digit product format
- 662670082
- Labeler code
- 66267
- Product ID
- 66267-082_9cbe7603-f6a3-5760-e053-2995a90acfd0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- diphenoxylate hydrochloride and atropine sulfate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- NuCare Pharmaceuticals, Inc.
- Application
- ANDA085762
- Marketing category
- ANDA
- Marketing start
- 1977-11-17
- Marketing end
- 0000-00-00
- Substance
- DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE
- Active strength
- 3 mg/1; mg/1
- Pharmacologic classes
- Antidiarrheal [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]
- DEA schedule
- CV
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 66267-082-20 | 66267008220 | 20 TABLET in 1 BOTTLE, PLASTIC (66267-082-20) | 20 tablet | 2016-09-30 | 0000-00-00 | No | No | Current |