NDC 0121-1746-30 - LACTULOSE
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
- 0121-1746
- Requested NDC
- 0121-1746-30
- Package NDCs from labels
- 0121-1746-30, 0121-1746-40, 0121-1746-00, 0121-1746-06
- Manufacturer
- PAI Holdings, LLC dba PAI Pharma | PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma
- Effective date
- 2025-09-15
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Lactulose Solution USP 10 g/15 mL | PAI Holdings, LLC dba PAI Pharma | PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma | 2025-09-15 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0121-1746-00 | LACTULOSE | 10 in 1 CASE | SOLUTION | 10 | 8 | |
| 0121-1746-00 | LACTULOSE | 10 in 1 TRAY | SOLUTION | 10 | 8 | |
| 0121-1746-06 | LACTULOSE | 16 in 1 CARTON | SOLUTION | 16 | 8 | |
| 0121-1746-06 | LACTULOSE | 6 in 1 CASE | SOLUTION | 6 | 8 | |
| 0121-1746-30 | LACTULOSE | 30 mL in 1 CUP, UNIT-DOSE | SOLUTION | 30 | 8 | |
| 0121-1746-40 | LACTULOSE | 4 in 1 CASE | SOLUTION | 4 | 8 | |
| 0121-1746-40 | LACTULOSE | 10 in 1 TRAY | SOLUTION | 10 | 8 |
DailyMed Dashboard NDC Coverage#
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 |
|---|---|---|---|---|---|---|
| Lactulose | LACTULOSE | American Health Packaging | 8b79d0d6-b9e3-436e-bab7-01451b6f45cd | 2026-08-17 | Warnings, Adverse reactions | 391937 9U7D5QH5AE |
| Lactulose Solution | LACTULOSE SOLUTION USP, 10 G/15 ML | Kesin Pharma Corporation | 163d5093-e35c-0bbf-e063-6294a90a803e | 2026-08-03 | Warnings, Adverse reactions | 391937 9U7D5QH5AE |
| Lactulose Solution | LACTULOSE SOLUTION USP, 10 G/15 ML | Kesin Pharma Corporation | 2d90e2a4-334f-ab68-e063-6294a90affa6 | 2026-08-03 | Warnings, Adverse reactions | 391937 9U7D5QH5AE |
| Lactulose | LACTULOSE | APOZEAL PHARMACEUTICALS INC | 72ac130a-de85-464d-9e9b-05cac0c54db1 | 2026-07-23 | Warnings, Adverse reactions | 391937 9U7D5QH5AE |
| Lactulose | LACTULOSE | PAI Holdings, LLC dba PAI Pharma | 5ae4b6da-44df-419a-9f2b-8c4d79f635c8 | 2026-07-07 | Warnings, Adverse reactions | 9U7D5QH5AE |
| LACTULOSE | LACTULOSE | Cardinal Health 107, LLC | 3cf3ff7c-67e7-42a9-8ebb-bd6c53937dd7 | 2026-05-19 | Warnings, Adverse reactions | ANDA074623 391937 9U7D5QH5AE |
| Lactulose | LACTULOSE | Xttrium Laboratories, Inc. | df62ad54-5aba-4d05-e053-2a95a90aa48d | 2026-04-14 | Warnings, Adverse reactions | 391937 9U7D5QH5AE |
| Lactulose | LACTULOSE | Chartwell RX, LLC | d6975cd8-80e0-43e2-809a-175ea7e40715 | 2026-01-28 | Warnings, Adverse reactions | 391937 9U7D5QH5AE |
| Lactulose Solution | LACTULOSE SOLUTION USP, 10 G/15 ML | Rising Pharma Holdings, Inc. | e75c335b-f19e-42e2-a24f-d891a52d3d34 | 2026-01-12 | Warnings, Adverse reactions | 391937 9U7D5QH5AE |
| Lactulose | LACTULOSE | APOZEAL PHARMACEUTICALS INC | a8af7389-3699-4873-b05a-509af7e8eaab | 2026-01-06 | Warnings, Adverse reactions | 391937 9U7D5QH5AE |
| Lactulose | LACTULOSE | Foxland Pharmaceuticals, Inc. | 3363bdbd-f0d1-45b3-8193-7fdb0a310cc2 | 2025-12-16 | Warnings, Adverse reactions | 9U7D5QH5AE |
| Lactulose | LACTULOSE | Chartwell RX, LLC. | bd9f1577-65e8-4521-b176-e5fc60a4a018 | 2025-12-08 | Warnings, Adverse reactions | 391937 9U7D5QH5AE |
| Lactulose | LACTULOSE | Chartwell Governmental & Specialty RX, LLC. | 887157ba-3c91-4fbf-bb12-b49c6fa4252c | 2025-11-13 | Warnings, Adverse reactions | 391937 9U7D5QH5AE |
| LACTULOSE | LACTULOSE | Atlantic Biologicals Corp. | 3fb6e908-893c-5a57-e063-6294a90a1bfc | 2025-09-26 | Warnings, Adverse reactions | ANDA074623 391937 9U7D5QH5AE |
| LACTULOSE | LACTULOSE | PAI Holdings, LLC dba PAI Pharma | 0f19e4ed-c90a-4330-a7fa-bf911aa98f09 | 2025-09-15 | Warnings, Adverse reactions | ANDA074623 391937 9U7D5QH5AE |
| LACTULOSE | LACTULOSE | PAI Holdings, LLC dba PAI Pharma | cbf0497c-9c8d-4dfa-bebd-64c589468401 | 2025-09-15 | Warnings, Adverse reactions | ANDA074623 0121-0873-15 0121-0873-16 0121-0873-08 0121-0873-32 0121-1746-00 0121-1746-40 0121-1746-06 0121-1746-30 0121-1746 0121-0873 00121174630 391937 b73c2ddc-a690-46e1-aa89-40fa890c9ab4 cbf0497c-9c8d-4dfa-bebd-64c589468401 9U7D5QH5AE |
| Lactulose | LACTULOSE | Trifluent Pharma, Inc. | 3eaf273a-b49d-2595-e063-6394a90a1cf6 | 2025-09-13 | Warnings, Adverse reactions | 9U7D5QH5AE |
| LACTULOSE Crystalline | LACTULOSE | Cumberland Assured Products Inc. | 59e75426-42ae-4904-941f-009181101a8a | 2025-09-01 | Warnings, Adverse reactions | 9U7D5QH5AE |
| Lactulose | LACTULOSE | Sun Pharmaceutical Industries, Inc. | 391cfd01-c1fa-41f9-abd7-d0abe9a27634 | 2025-08-04 | Warnings, Adverse reactions | 391937 9U7D5QH5AE |
| Enulose | LACTULOSE | Bryant Ranch Prepack | fa3aae7c-6f98-4fbb-85dc-32affe9874d5 | 2024-12-18 | Warnings, Adverse reactions | 391937 9U7D5QH5AE |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.