bimatoprost
- Product NDC
- 68180-429
- 11-digit product format
- 681800429
- Labeler code
- 68180
- Product ID
- 68180-429_c8bcbc68-7043-4f85-8e07-455d77e595bc
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- bimatoprost
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- Lupin Pharmaceuticals, Inc.
- Application
- ANDA203991
- Marketing category
- ANDA
- Marketing start
- 2015-05-13
- Marketing end
- 0000-00-00
- Substance
- BIMATOPROST
- Active strength
- 0 mg/mL
- Pharmacologic classes
- Prostaglandin Analog [EPC], Prostaglandins [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68180-429-01 | 68180042901 | 1 BOTTLE, DROPPER in 1 CARTON (68180-429-01) > 2.5 mL in 1 BOTTLE, DROPPER | 2015-05-13 | 0000-00-00 | No | No | Current |
| 68180-429-02 | 68180042902 | 1 BOTTLE, DROPPER in 1 CARTON (68180-429-02) > 5 mL in 1 BOTTLE, DROPPER | 2015-05-13 | 0000-00-00 | No | No | Current |
| 68180-429-03 | 68180042903 | 1 BOTTLE, DROPPER in 1 CARTON (68180-429-03) > 7.5 mL in 1 BOTTLE, DROPPER | 2015-05-13 | 0000-00-00 | No | No | Current |