Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate and Scopolamine Hydrobromide
- Product NDC
- 66993-117
- 11-digit product format
- 669930117
- Labeler code
- 66993
- Product ID
- 66993-117_d277bc11-b90b-4a18-986e-fb995ffdbea0
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate and Scopolamine Hydrobromide
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Prasco Laboratories
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2019-11-18
- Marketing end
- 2021-11-30
- Substance
- PHENOBARBITAL; HYOSCYAMINE SULFATE; ATROPINE SULFATE; SCOPOLAMINE HYDROBROMIDE
- Active strength
- 16 mg/1; mg/1; mg/1; mg/1
- Pharmacologic classes
- Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA]
- DEA schedule
- CIV
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- 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 |
|---|
| 66993-117-02 | 66993011702 | 100 TABLET in 1 BOTTLE, PLASTIC (66993-117-02) | 100 tablet | 2019-11-18 | 0000-00-00 | No | No | Current |