Bimatoprost
- Product NDC
- 72266-241
- 11-digit product format
- 722660241
- Labeler code
- 72266
- Product ID
- 72266-241_2c7970dc-8873-7e74-e063-6294a90a397f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bimatoprost
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Fosun Pharma USA Inc.
- Application
- ANDA210126
- Marketing category
- ANDA
- Marketing start
- 2025-11-30
- Substance
- BIMATOPROST
- Active strength
- .3 mg/mL
- Pharmacologic classes
- Prostaglandin Analog [EPC], Prostaglandins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bimatoprost
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BIMATOPROST | .3 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | QXS94885MZ |
| Rxcui | 308739 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72266-241-01 | Bimatoprost | 7.5 mL in 1 BOTTLE | SOLUTION/ DROPS | 7.5 | | 6 |
| 72266-241-01 | Bimatoprost | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72266-241 | BIMATOPROST SOLUTION/ DROPS [FOSUN PHARMA USA INC.] | 5 | Current NDC, Legacy NDC, 2 package rows | 20250110_2f9ee30a-1737-44b2-8479-79a3ee88bf5b.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72266-241-01 | 72266024101 | 1 BOTTLE in 1 CARTON (72266-241-01) / 7.5 mL in 1 BOTTLE | 1 bottle | 2025-11-30 | 0000-00-00 | No | No | Current |