Pretomanid 200 mg / 1 Tablet 1 Bottle
Reference details for licensed healthcare facility review and verification.
| NDC 11 | 49502-0476-26 |
|---|---|
| Product NDC | 49502-0476 |
| Generic Drug Name | Pretomanid |
| Brand Name | Pretomanid |
| Manufacturer | Viatris Specialty LLC |
| Strength | 200 mg / 1 |
| Dosage Form | Tablet |
| Drug Type | Oral |
| Package Quantity | 1 Bottle |
| Package Description | 1 BOTTLE in 1 CARTON (49502-476-26) / 26 TABLET in 1 BOTTLE |
| Active Ingredients | Pretomanid |
| Marketing Category | NDA |
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NDC snapshot
Pretomanid 200 mg / 1 Tablet is tracked under NDC 49502-0476-26 and rolls up into product family 49502-0476. Use this page to review package-level identifiers before comparing related family pages or starting a quote review.
- Package configuration: 1 Bottle.
- Manufacturer: Viatris Specialty LLC.
- Dosage form: Tablet.
- Family size: 1 indexed presentation.
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Official references
Use official labeling and directory references to confirm presentation details while your team reviews the PRN catalog entry and related sourcing paths.
Pretomanid 200 mg / 1 Tablet 1 Bottle, NDC 49502-0476-26, is a Viatris Specialty LLC 200 mg / 1 tablet presentation packaged as 1 Bottle.
NDC search formats
- Canonical NDC 11: 49502-0476-26
- Digits-only NDC 11: 49502047626
- Possible 10-digit display format: 49502-476-26 (4950247626)
Helpful product links
- Search by brand name: Pretomanid
- NDC 11: 49502-0476-26
- Product family NDC: 49502-0476
- VA classification code: AM500
- VA classification code description: ANTITUBERCULARS
- CMOP ID: P1254
- VUID: 4038960