Baricitinib 4 mg / 1 Tablet 30 Tablet, Film Coated
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 00002-6885-30 |
|---|---|
| Product NDC | 00002-6885 |
| Generic Drug Name | baricitinib |
| Brand Name | Baricitinib |
| Manufacturer | Eli Lilly and Company |
| Strength | 4 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 30 Tablet, Film Coated |
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (0002-6885-30) |
| Active Ingredients | Baricitinib |
| Marketing Category | EMERGENCY USE AUTHORIZATION |
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NDC snapshot
baricitinib 4 mg / 1 Tablet is tracked under NDC 00002-6885-30 and rolls up into product family 00002-6885. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 30 Tablet, Film Coated.
- Manufacturer: Eli Lilly and Company.
- Dosage form: Tablet.
- Family size: 1 indexed presentation.
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Official references
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Potential alternatives with matching presentation
Open the comparison hub or review package-level listings from 2 product-NDC families with matching normalized presentation details. Review each product detail page before treating any item as a true alternative.
Baricitinib 4 mg / 1 Tablet 30 Tablet, Film Coated, NDC 00002-6885-30, is a Eli Lilly and Company 4 mg / 1 tablet presentation packaged as 30 Tablet, Film Coated.
NDC search formats
- Canonical NDC 11: 00002-6885-30
- Digits-only NDC 11: 00002688530
- Possible 10-digit display format: 0002-6885-30 (0002688530)
Helpful product links
- Search by brand name: Baricitinib
- NDC 11: 00002-6885-30
- Product family NDC: 00002-6885