Maraviroc
- Product NDC
- 68475-008
- 11-digit product format
- 684750008
- Labeler code
- 68475
- Product ID
- 68475-008_9623d31f-0856-4aca-a288-c542b28edfba
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Maraviroc
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Navinta LLC
- Application
- ANDA217880
- Marketing category
- ANDA
- Marketing start
- 2025-06-23
- Substance
- MARAVIROC
- Active strength
- 150 mg/1
- Pharmacologic classes
- CCR5 Co-receptor Antagonist [EPC], Chemokine Co-receptor 5 Antagonists [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Maraviroc
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MARAVIROC | 150 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | MD6P741W8A |
| Rxcui | 728223, 728225 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68475-008-01 | Maraviroc | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 68475-008-01 | 68475000801 | 60 TABLET, FILM COATED in 1 BOTTLE (68475-008-01) | 2025-06-23 | No | No | Historical |