Prescription drug · UNAPPROVED DRUG OTHER
Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide NDC 50742-666
Phenobarbital 16.2 mg/5mL + 3 more ingredients · Elixir · Oral · Ingenus Pharmaceuticals, LLC
NDC codes
FDA NDC Directory| Package NDC | 11-digit (billing) | Package | Copy |
|---|---|---|---|
| 50742-666-04 | 5074206660450742066604 | 118 mL in 1 BOTTLE (50742-666-04)Marketed from Aug 1, 2021 | |
| 50742-666-16 | 5074206661650742066616 | 473 mL in 1 BOTTLE (50742-666-16)Marketed from Aug 1, 2021 |
How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules
Product information
- Brand name (proprietary)
- Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide
- Generic name (nonproprietary)
- phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide
- Active ingredients
- Phenobarbital — 16.2 mg/5mLHyoscyamine sulfate — .1037 mg/5mLAtropine sulfate — .0194 mg/5mLScopolamine hydrobromide — .0065 mg/5mL
- Dosage form
- Elixir
- Route
- Oral
- Labeler
- Ingenus Pharmaceuticals, LLCNDC labeler code 50742
- Product type
- Prescription drug
- Marketing category
- Unapproved drug (other)
- Marketing start
- Listing expires
- DEA schedule
- CIV
- Other FDA classes
- Cholinergic Antagonists (Mechanism)Cholinergic Antagonists (Mechanism)Cholinergic Muscarinic Antagonists (Mechanism)
- Identifiers
- Product ID 50742-666_5e9a2654-23e8-43de-a8fa-d981d7f13e40SPL ID 5e9a2654-23e8-43de-a8fa-d981d7f13e40SPL set ID 33bf2df5-bc53-4d57-a9e7-41f3fc0a03f0RxCUI 1046787UNII F2R8V82B84, YQE403BP4D, 451IFR0GXB, 03J5ZE7KA5UPC 0350742665167, 0350742665044, 0350742666041
- Pharmacologic class
- Anticholinergic; Cholinergic Muscarinic Antagonist
Billing references
What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.
- HCPCS codeNo match
No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.
- NDC on a medical claim
N450742066604followed by a unit qualifier and the quantityPackage 50742-0666-04. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier
Product label
Current FDA label (SPL), effective .
About NDC 50742-666
- What is NDC 50742-666?
- 50742-666 is the product NDC for Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide, Phenobarbital 16.2 mg/5mL + 3 more ingredients elixir, listed with the FDA by Ingenus Pharmaceuticals, LLC. It has 2 package NDCs, shown above in 10- and 11-digit form.
- What drug is associated with this NDC?
- Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide.
- What is the active ingredient?
- Phenobarbital, Hyoscyamine sulfate, Atropine sulfate, Scopolamine hydrobromide.
- Who is the labeler?
- Ingenus Pharmaceuticals, LLC, NDC labeler code 50742. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
- What other NDCs exist for Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide?
- 1 other product NDC are listed under this name. See all Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide NDCs.
- Is there a related HCPCS / J-code?
- Not in Med-Code's curated HCPCS directory. See Billing references above.
Related NDCs: other Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide products
Other finished products listed under the same name: strengths, forms and labelers.
| Product | Strength | Form · route | Labeler | Product NDC | Package NDCs (11-digit) |
|---|---|---|---|---|---|
| Phenobarbital, Hyoscyamine Sulfate, Atropine Sulfate, Scopolamine Hydrobromide | Phenobarbital 16.2 mg/5mL + 3 more ingredients | ElixirOral | Ingenus Pharmaceuticals, LLC | 50742-665 | 50742-0665-0450742-0665-16 |