Bimatoprost
- Product NDC
- 70756-628
- 11-digit product format
- 707560628
- Labeler code
- 70756
- Product ID
- 70756-628_4ba103dc-872b-49f0-ae33-f1fc4b98c776
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Bimatoprost
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Lifestar Pharma LLC
- Application
- ANDA218196
- Marketing category
- ANDA
- Marketing start
- 2026-03-17
- Substance
- BIMATOPROST
- Active strength
- .1 mg/mL
- Pharmacologic classes
- Prostaglandin Analog [EPC], Prostaglandins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Bimatoprost
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| BIMATOPROST | .1 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | QXS94885MZ |
| Rxcui | 1009339 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70756-628-30 | Bimatoprost | 7.5 mL in 1 BOTTLE | SOLUTION/ DROPS | 7.5 | | 4 |
| 70756-628-30 | Bimatoprost | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | | 4 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70756-628-30 | 70756062830 | 1 BOTTLE in 1 CARTON (70756-628-30) / 7.5 mL in 1 BOTTLE | 1 bottle | 2026-03-17 | No | No | Current |