NDC 17856-0162

PHENOBARBITAL WITH BELLADONNA ALKALOIDS

Phenobarbital With Belladonna Alkaloids

PHENOBARBITAL WITH BELLADONNA ALKALOIDS is a Oral Elixir in the Human Prescription Drug category. It is labeled and distributed by Atlantic Biologicals Corp.. The primary component is Phenobarbital; Hyoscyamine Sulfate; Atropine Sulfate; Scopolamine Hydrobromide.

• Product ID: 17856-0162_ff8788e9-0855-4f9d-9a22-84f3e18ef3b3
• NDC: 17856-0162
• Product Type: Human Prescription Drug
• Proprietary Name: PHENOBARBITAL WITH BELLADONNA ALKALOIDS
• Generic Name: Phenobarbital With Belladonna Alkaloids
• Dosage Form: Elixir
• Route of Administration: ORAL
• Marketing Start Date: 2018-05-21
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: ATLANTIC BIOLOGICALS CORP.
• Substance Name: PHENOBARBITAL; HYOSCYAMINE SULFATE; ATROPINE SULFATE; SCOPOLAMINE HYDROBROMIDE
• Active Ingredient Strength: 16 mg/5mL; mg/5mL; mg/5mL; mg/5mL
• Pharm Classes: Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA],Anticholinergic [EPC],Cholinergic Antagonists [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2019-12-31

Packaging

NDC 17856-0162-1

10 mL in 1 CUP, UNIT-DOSE (17856-0162-1)

• Marketing Start Date: 2018-06-15
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 17856-0162-2 [17856016202]

PHENOBARBITAL WITH BELLADONNA ALKALOIDS ELIXIR

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-06-15
• Inactivation Date: 2020-01-31

NDC 17856-0162-4 [17856016204]

PHENOBARBITAL WITH BELLADONNA ALKALOIDS ELIXIR

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-06-15
• Inactivation Date: 2020-01-31

NDC 17856-0162-1 [17856016201]

PHENOBARBITAL WITH BELLADONNA ALKALOIDS ELIXIR

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-06-15
• Inactivation Date: 2020-01-31

NDC 17856-0162-3 [17856016203]

PHENOBARBITAL WITH BELLADONNA ALKALOIDS ELIXIR

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Marketing Start Date: 2018-06-15
• Inactivation Date: 2020-01-31

Drug Details

Active Ingredients

Ingredient	Strength
PHENOBARBITAL	16.2 mg/5mL

OpenFDA Data

• SPL SET ID: 6186eca3-be71-48d6-b102-de15746f49e7
• Manufacturer:
  • ATLANTIC BIOLOGICALS CORP.
• UNII:
  • YQE403BP4D
  • 451IFR0GXB
  • 03J5ZE7KA5
  • F2R8V82B84
• RxNorm Concept Unique ID - RxCUI:
  • 1046787

Pharmacological Class

• Anticholinergic [EPC]
• Cholinergic Antagonists [MoA]
• Cholinergic Muscarinic Antagonist [EPC]
• Cholinergic Muscarinic Antagonists [MoA]
• Anticholinergic [EPC]
• Cholinergic Antagonists [MoA]

NDC Crossover Matching brand name "PHENOBARBITAL WITH BELLADONNA ALKALOIDS" or generic name "Phenobarbital With Belladonna Alkaloids"

NDC	Brand Name	Generic Name
17856-0162	PHENOBARBITAL WITH BELLADONNA ALKALOIDS	PHENOBARBITAL WITH BELLADONNA ALKALOIDS
42291-205	PHENOBARBITAL WITH BELLADONNA ALKALOIDS	PHENOBARBITAL WITH BELLADONNA ALKALOIDS
63629-2003	PHENOBARBITAL WITH BELLADONNA ALKALOIDS	PHENOBARBITAL WITH BELLADONNA ALKALOIDS
63629-2004	PHENOBARBITAL WITH BELLADONNA ALKALOIDS	PHENOBARBITAL WITH BELLADONNA ALKALOIDS
63629-2005	PHENOBARBITAL WITH BELLADONNA ALKALOIDS	PHENOBARBITAL WITH BELLADONNA ALKALOIDS
63629-2050	Phenobarbital with Belladonna Alkaloids	phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide
71914-162	PHENOBARBITAL WITH BELLADONNA ALKALOIDS	PHENOBARBITAL WITH BELLADONNA ALKALOIDS
72768-7010	Phenobarbital with Belladonna Alkaloids	phenobarbital, hyoscyamine sulfate, atropine sulfate, scopolamine hydrobromide