NDC 76420-782

Marbeta L Kit

Betamethasone Sodium Phosphate, Betamethasone Acetate, Lidocaine Hydrochloride, Bupivacaine Hydrochloride, Povidine Iodine, Isopropyl Alcohol

Marbeta L Kit is a Epidural; Infiltration; Intra-articular; Intralesional; Intramuscular; Topical Kit in the Human Prescription Drug category. It is labeled and distributed by Asclemed Usa, Inc.. The primary component is .

• Product ID: 76420-782_7b291076-365f-9793-e053-2991aa0a9f53
• NDC: 76420-782
• Product Type: Human Prescription Drug
• Proprietary Name: Marbeta L Kit
• Generic Name: Betamethasone Sodium Phosphate, Betamethasone Acetate, Lidocaine Hydrochloride, Bupivacaine Hydrochloride, Povidine Iodine, Isopropyl Alcohol
• Dosage Form: Kit
• Route of Administration: EPIDURAL; INFILTRATION; INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; TOPICAL
• Marketing Start Date: 2010-04-28
• Marketing Category: UNAPPROVED DRUG OTHER / UNAPPROVED DRUG OTHER
• Labeler Name: Asclemed USA, Inc.
• Active Ingredient Strength: 0
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 76420-782-01

1 KIT in 1 CARTON (76420-782-01) * 1 VIAL, MULTI-DOSE in 1 CARTON (0517-0720-01) > 5 mL in 1 VIAL, MULTI-DOSE * 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-162-05) > 5 mL in 1 VIAL, SINGLE-DOSE * 25 VIAL, SINGLE-DOSE in 1 CARTON (55150-167-10) > 10 mL in 1 VIAL, SINGLE-DOSE * 5 mL in 1 POUCH * .9 mL in 1 PACKET (67777-419-02)

• Marketing Start Date: 2016-05-23
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 76420-782-01 [76420078201]

Marbeta L Kit KIT

• Marketing Category: unapproved drug other
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-05-23

Drug Details

OpenFDA Data

• SPL SET ID: 9a6a3871-4e02-47f9-a20e-a256b3f3c498
• Manufacturer:
  • Asclemed USA, Inc.
• RxNorm Concept Unique ID - RxCUI:
  • 797544
  • 1725078
  • 1737566
  • 578803
  • 797730