Maraviroc
- Product NDC
- 70710-1931
- 11-digit product format
- 707101931
- Labeler code
- 70710
- Product ID
- 70710-1931_b9cfbc86-86a5-487f-8b6d-1e9607d2f8f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Maraviroc
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Application
- ANDA217880
- Marketing category
- ANDA
- Marketing start
- 2025-05-23
- Substance
- MARAVIROC
- Active strength
- 300 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 | 300 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 |
|---|
| 70710-1931-6 | Maraviroc | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | | 1 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70710-1931 | MARAVIROC TABLET, FILM COATED [ZYDUS PHARMACEUTICALS USA INC.] | 1 | Current NDC, 1 package rows | 20250523_9bba17ba-0bc5-430c-96d1-c568e236a0ed.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 70710-1931-6 | 70710193106 | 60 TABLET, FILM COATED in 1 BOTTLE (70710-1931-6) | 2025-05-23 | No | No | Historical |