NDC 0187-4220

Seconal Sodium

Secobarbital Sodium

Seconal Sodium is a Oral Capsule in the Human Prescription Drug category. It is labeled and distributed by Bausch Health Us, Llc. The primary component is Secobarbital Sodium.

• Product ID: 0187-4220_4a71fd6c-feaa-4412-934a-60d1d477d50b
• NDC: 0187-4220
• Product Type: Human Prescription Drug
• Proprietary Name: Seconal Sodium
• Generic Name: Secobarbital Sodium
• Dosage Form: Capsule
• Route of Administration: ORAL
• Marketing Start Date: 1983-10-03
• Marketing Category: ANDA / ANDA
• Application Number: ANDA086101
• Labeler Name: Bausch Health US, LLC
• Substance Name: SECOBARBITAL SODIUM
• Active Ingredient Strength: 100 mg/1
• DEA Schedule: CII
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 0187-4220-10

100 CAPSULE in 1 BOTTLE (0187-4220-10)

• Marketing Start Date: 1983-10-03
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 0187-4220-10 [00187422010]

Seconal Sodium CAPSULE

• Marketing Category: ANDA
• Application Number: ANDA086101
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 1983-10-03

Drug Details

Active Ingredients

Ingredient	Strength
SECOBARBITAL SODIUM	100 mg/1

OpenFDA Data

• SPL SET ID: d892a312-12ba-4d32-a840-2c0ff3dc1d58
• Manufacturer:
  • Valeant Pharmaceuticals North America LLC
• UNII:
  • XBP604F6UM
• RxNorm Concept Unique ID - RxCUI:
  • 312914
  • 201625