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NDC 76420-0796-01 Dyural 80-LM Details
Dyural 80-LM
Dyural 80-LM is a EPIDURAL; INFILTRATION; INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE; SUBCUTANEOUS; TOPICAL KIT in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Asclemed USA, Inc.. The primary component is .
Product Information
| NDC | 76420-0796 |
|---|---|
| Product ID | 76420-796_efdc0036-fb4f-369b-e053-2a95a90aa50f |
| Associated GPIs | 22109903506440 |
| GCN Sequence Number | n/a |
| GCN Sequence Number Description | n/a |
| HIC3 | n/a |
| HIC3 Description | n/a |
| GCN | n/a |
| HICL Sequence Number | n/a |
| HICL Sequence Number Description | n/a |
| Brand/Generic | n/a |
| Proprietary Name | Dyural 80-LM |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Methylprednisolone Acetate, Lidocaine Hydrochloride, Bupivacaine Hydrochloride, Povidine Iodine, Isopropyl Alcohol |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | KIT |
| Route | EPIDURAL; INFILTRATION; INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR; INTRAVENOUS; SOFT TISSUE; SUBCUTANEOUS; TOPICAL |
| Active Ingredient Strength | n/a |
| Active Ingredient Units | n/a |
| Substance Name | n/a |
| Labeler Name | Asclemed USA, Inc. |
| Pharmaceutical Class | n/a |
| DEA Schedule | n/a |
| Marketing Category | UNAPPROVED DRUG OTHER |
| Application Number | n/a |
| Listing Certified Through | 2024-12-31 |
Package
NDC 76420-0796-01 (76420079601)
| NDC Package Code | 76420-796-01 |
|---|---|
| Billing NDC | 76420079601 |
| Package | 1 KIT in 1 CARTON (76420-796-01) * 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-162-05) / 5 mL in 1 VIAL, SINGLE-DOSE * 10 mL in 1 VIAL, SINGLE-DOSE (0409-1159-18) * .9 mL in 1 PACKET (67777-419-02) * 1 VIAL, SINGLE-DOSE in 1 CARTON (70121-1574-1) / 1 |
| Marketing Start Date | 2022-01-11 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |