NDC 50742-666 – Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide
Phenobarbital 16.2 mg/5mL; Hyoscyamine Sulfate .1037 mg/5mL; Atropine Sulfate .0194 mg/5mL; Scopolamine Hydrobromide .0065 mg/5mL · Elixir · Oral
Product NDC50742-666
Product details
- Brand name
- Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide
- Generic name
- Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide
- Labeler
- Ingenus Pharmaceuticals, LLC
- Dosage form
- Elixir
- Route
- Oral
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketed since
- August 1, 2021
- Listing expires
- December 31, 2026
- Pharmacologic class
- Anticholinergic; Anticholinergic; Cholinergic Muscarinic Antagonist
Active ingredients
- Phenobarbital 16.2 mg/5mL
- Hyoscyamine Sulfate .1037 mg/5mL
- Atropine Sulfate .0194 mg/5mL
- Scopolamine Hydrobromide .0065 mg/5mL
Package NDC codes (2)
| Package NDC | Description | Since |
|---|---|---|
| 50742-666-04 | 118 mL in 1 BOTTLE (50742-666-04) | Aug 1, 2021 |
| 50742-666-16 | 473 mL in 1 BOTTLE (50742-666-16) | Aug 1, 2021 |
Other Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide products
- 50742-665 Phenobarbital 16.2 mg/5mL; Hyoscyamine Sulfate .1037 mg/5mL; Atropine… · Elixir · Ingenus Pharmaceuticals, LLC