NDC 60219-2149-01 - Bimatoprost
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 60219-2149
- Requested NDC
- 60219-2149-01
- Package NDCs from labels
- 60219-2149-1, 60219-2149-4, 60219-2149-2, 60219-2149-01
- Manufacturer
- Amneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals Private Limited
- Effective date
- 2025-05-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Bimatoprost - Amneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals Private Limited | Amneal Pharmaceuticals NY LLC | Amneal Pharmaceuticals Private Limited | 2025-05-24 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 60219-2149-1 | Bimatoprost | 2.5 mL in 1 BOTTLE | SOLUTION/ DROPS | 2.5 | 4 | |
| 60219-2149-1 | Bimatoprost | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | 4 | |
| 60219-2149-2 | Bimatoprost | 7.5 mL in 1 BOTTLE | SOLUTION/ DROPS | 7.5 | 4 | |
| 60219-2149-2 | Bimatoprost | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | 4 | |
| 60219-2149-4 | Bimatoprost | 5 mL in 1 BOTTLE | SOLUTION/ DROPS | 5 | 4 | |
| 60219-2149-4 | Bimatoprost | 1 in 1 CARTON | SOLUTION/ DROPS | 1 | 4 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 60219-2149-1 | ML - Milliliter | 60219-2149 | 044c816b-8a94-4d40-9f07-116532cdfc0f | 1 | 2026-04-20 |
| 60219-2149-2 | ML - Milliliter | 60219-2149 | a115007b-c038-4572-a7a9-f57f8546240e | 1 | 2026-04-20 |
| 60219-2149-4 | ML - Milliliter | 60219-2149 | 1afbd3a2-4446-4014-8d9e-0fbcdb85e5ff | 1 | 2026-04-20 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| Dial Antibacterial Defense Gold | BENZALKONIUM CHLORIDE | Henkel Corporation | 0a34b1b4-ad14-43b7-e063-6394a90a570f | 2025-11-24 | Warnings | F5UM2KM3W7 |
| CLASSIC TOUCH Antibacterial Plum Foam Handwash | BENZALKONIUM CHLORIDE | AFFLAB, Affiliated Laboratories, a Division of AFFLINK | 7b406cfa-fa50-4512-81a1-7eb16b50dd1f | 2025-11-24 | Warnings | F5UM2KM3W7 |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | beda35c3-9a8b-47ad-e053-2995a90a7b1b | 2025-11-24 | Warnings | 059QF0KO0R |
| Easy Care First Aid Eyewash | WATER | Tender Corporation | a070aac8-e6d2-ef10-e053-2a95a90aa5b1 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | e07a064b-f680-405c-bbcd-24fac430951e | 2025-11-24 | Warnings | 059QF0KO0R |
| ULINE Eyewash | EYEWASH | Niagara Pharmaceuticals Inc. | 2d7f22d2-320b-6af1-e063-6294a90addc6 | 2025-11-24 | Warnings | 059QF0KO0R |
| Pur-Wash | EYEWASH | Niagara Pharmaceuticals, Inc. | 0d43b1c1-2699-37f1-e054-00144ff88e88 | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 777e1559-786f-8d54-e053-2991aa0aa98d | 2025-11-24 | Warnings | 059QF0KO0R |
| PUR-WASH | WATER | Niagara Pharmaceuticals Inc. | 7289103a-5cbf-42f4-8848-e827149a43ca | 2025-11-24 | Warnings | 059QF0KO0R |
| Natural Eyes Floaters Relief | CHELIDONIUM, EUPHRASIA, KALI SULPH, NATRUM MURIATICUM, PHOSPHORUS, PHYSOSTIGMA, SEPIA, SILICEA | TRP Company | 445dc831-195e-4b25-e063-6294a90a6efd | 2025-11-24 | Warnings | 451W47IQ8X |
| Protex Balance antibacterial hand | BENZALKONIUM CHLORIDE | Colgate-Palmolive Company | d2514b67-303a-40f4-867b-9f41c0c8cba8 | 2025-11-24 | Warnings | F5UM2KM3W7 |
| FloraMedis Hand Sanitizer | HAND SANITIZER | Sichuan Pengtai Qifan Technology Co., Ltd | 4415ca9f-10b1-88f7-e063-6294a90a2e09 | 2025-11-21 | Warnings | F5UM2KM3W7 |
| DG 4x Medicated Tooth and Gum Cream | BENZOCAINE | Dollar General | b2c156f0-6d11-1eba-e053-2995a90a6db8 | 2025-11-21 | Warnings | F5UM2KM3W7 |
| 4x Medicated Toothache and Gum Gel | BENZOCAINE | CVS | a7577d5f-69cf-3f32-e053-2995a90aaba5 | 2025-11-21 | Warnings | F5UM2KM3W7 |
| Nighttime 4X Medicated Cream | BENZOCAINE | Rite Aid | 21645ed1-2dc0-223a-e063-6394a90ab021 | 2025-11-21 | Warnings | F5UM2KM3W7 |
| 4x Medicated Gum Cream | BENZOCAINE | Albertsons | b81a308c-9c30-0e3d-e053-2a95a90a15d2 | 2025-11-21 | Warnings | F5UM2KM3W7 |
| pre fense | BENZALKONIUM CHLORIDE | Prefense LLC | fad70060-8bb6-4b06-a353-666132f64c26 | 2025-11-21 | Warnings | F5UM2KM3W7 |
| pre fense unscented | BENZALKONIUM CHLORIDE | Prefense LLC | a59e9bbf-b60e-970a-e053-2a95a90aaa5e | 2025-11-21 | Warnings | F5UM2KM3W7 |
| Candida HP | BAPTISIA TINCTORIA ROOT, ECHINACEA PURPUREA, GLYCYRRHIZA GLABRA, ASTRAGALUS NUTTALLII LEAF, CANDIDA ALBICANS, SODIUM BORATE, OYSTER SHELL CALCIUM CARBONATE, CRUDE, WOOD CREOSOTE, LYCOPODIUM CLAVATUM SPORE, STRYCHNOS NUX-VOMICA SEED, PHOSPHORIC ACID, ANEMONE PULSATILLA, SEPIA OFFICINALIS JUICE, THUJA OCCIDENTALIS LEAFY TWIG, SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE, NITRIC ACID | Natural Creations, Inc. | b587a3f0-628b-41f7-8afb-2cdcd896279e | 2025-11-20 | Warnings | 70WT22SF4B |
| Eyewash Additive Concentrate | WATER AND PROPYLENE GLYCOL | Haws Corporation | dd168403-398c-41ff-b1df-d93e4ff39de3 | 2025-11-20 | Warnings | 059QF0KO0R |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.