NDC 71335-1007-01 - Gabapentin
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
- 71335-1007
- Requested NDC
- 71335-1007-01
- Package NDCs from labels
- 71335-1007-1, 71335-1007-2, 71335-1007-3, 71335-1007-4, 71335-1007-5, 71335-1007-6, 71335-1007-7, 71335-1007-8, 71335-1007-9, 71335-1007-01
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2024-04-09
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Gabapentin - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-04-09 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71335-1007-1 | Gabapentin | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 7 | |
| 71335-1007-2 | Gabapentin | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 7 | |
| 71335-1007-3 | Gabapentin | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 7 | |
| 71335-1007-4 | Gabapentin | 180 in 1 BOTTLE | TABLET, FILM COATED | 180 | 7 | |
| 71335-1007-5 | Gabapentin | 120 in 1 BOTTLE | TABLET, FILM COATED | 120 | 7 | |
| 71335-1007-6 | Gabapentin | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 7 | |
| 71335-1007-7 | Gabapentin | 84 in 1 BOTTLE | TABLET, FILM COATED | 84 | 7 | |
| 71335-1007-8 | Gabapentin | 112 in 1 BOTTLE | TABLET, FILM COATED | 112 | 7 | |
| 71335-1007-9 | Gabapentin | 135 in 1 BOTTLE | TABLET, FILM COATED | 135 | 7 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71335-1007 | GABAPENTIN TABLET, FILM COATED [BRYANT RANCH PREPACK] | 7 | Current NDC, Legacy NDC, 9 package rows | 20240410_47f2a06f-4eac-4dca-aa2a-a36dd4daaea0.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71335-1007-1 | EA - Each | 71335-1007 | f2b25697-1f03-47d4-94fe-7a0995686db5 | 1 | 2021-07-15 |
| 71335-1007-2 | EA - Each | 71335-1007 | b791aa29-3ce5-4638-b5e7-da655acfdcb7 | 1 | 2021-07-15 |
| 71335-1007-3 | EA - Each | 71335-1007 | 52c93a4e-79e2-4248-9daf-9bd9eada6690 | 1 | 2019-09-05 |
| 71335-1007-5 | EA - Each | 71335-1007 | 9f3e7833-80d9-47e1-a2f1-b44d11da9d70 | 1 | 2019-09-05 |
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 |
|---|---|---|---|---|---|---|
| Gabapentin | GABAPENTIN | NuCare Pharmaceuticals, Inc. | 57383d2a-d2c7-bbdc-e063-6294a90ada98 | 2026-07-22 | Warnings, Adverse reactions | 310434 6CW7F3G59X |
| GOOD NEIGHBOR PHARMACY ARTIFICAL TEARS LUBRICANT EYE DROPS | POLYVINYL ALCOHOL, POVIDONE | AmerisourceBergen | ce6852a8-c5e6-403d-a7b4-a2e85d1ebb1f | 2026-07-22 | Warnings | 532B59J990 |
| Yves Saint Laurent All Hours Foundation Sunscreen Broad Spectrum SPF 30 Luminous Matte Foundation | OCTINOXATE AND TITANIUM DIOXIDE | SICOS ET CIE | 571f23e9-1126-e32d-e063-6294a90a9951 | 2026-07-21 | Warnings | 15FIX9V2JP |
| Gabapentin | GABAPENTIN | ScieGen Pharmaceuticals, Inc. | 16542ee6-0e0e-4d3c-8b32-60ff6ef48846 | 2026-07-21 | Warnings, Adverse reactions | 6CW7F3G59X |
| MENS SPF50 ALL IN ONE SUNSCREEN | MENS SPF50 ALL IN ONE SUNSCREEN | Lance (Guangzhou) Biological Technology Co., Ltd. | 57074480-77fd-cc06-e063-6294a90a28d4 | 2026-07-20 | Warnings | 15FIX9V2JP |
| gabapentin | GABAPENTIN | REMEDYREPACK INC. | 32169228-e85c-4dbf-8722-cd2f8e0f5d1a | 2026-07-20 | Warnings, Adverse reactions | 6CW7F3G59X |
| Yves Saint Laurent All Hours Foundation Sunscreen Broad Spectrum SPF 30 Luminous Matte Foundation | OCTINOXATE AND TITANIUM DIOXIDE | L'Oreal USA Products Inc | 5711364c-f9b4-bfa6-e063-6294a90ace4a | 2026-07-20 | Warnings | 15FIX9V2JP |
| Gabapentin | GABAPENTIN | PD-Rx Pharmaceuticals, Inc. | 4a95f18e-0de4-4ce1-9f97-bc2e8a5bac6a | 2026-07-17 | Warnings, Adverse reactions | 6CW7F3G59X |
| Gabapentin | GABAPENTIN | St. Mary's Medical Park Pharmacy | 3c585b71-5cfc-18d6-e063-6294a90a3dcf | 2026-07-17 | Warnings, Adverse reactions | 6CW7F3G59X |
| Gabapentin | GABAPENTIN | Bryant Ranch Prepack | 172776c0-909e-49ce-bfe1-cf154a9458ba | 2026-07-15 | Warnings, Adverse reactions | 310434 6CW7F3G59X |
| Gabapentin | GABAPENTIN | Bryant Ranch Prepack | a1006139-7dfc-4d87-a5a9-aeb380c32d24 | 2026-07-15 | Warnings, Adverse reactions | 6CW7F3G59X |
| Gabapentin | GABAPENTIN | Bryant Ranch Prepack | df9c7c84-a8d9-4da8-babe-c55c9420d4e6 | 2026-07-15 | Warnings, Adverse reactions | 6CW7F3G59X |
| Gabapentin | GABAPENTIN | REMEDYREPACK INC. | 6beed8eb-446c-4575-8dc8-b798623d92c7 | 2026-07-15 | Warnings, Adverse reactions | 6CW7F3G59X |
| Gabapentin | GABAPENTIN | REMEDYREPACK INC. | 7ddc7d92-9076-41cf-97ed-d9f9edc80298 | 2026-07-15 | Warnings, Adverse reactions | 6CW7F3G59X |
| Gabapentin | GABAPENTIN | Bryant Ranch Prepack | 72729513-bd34-44f5-9f62-297ed25c4442 | 2026-07-15 | Warnings, Adverse reactions | 6CW7F3G59X |
| Gabapentin | GABAPENTIN | Bryant Ranch Prepack | f31172a2-0ae9-49f2-b797-b26fe33f3f64 | 2026-07-15 | Warnings, Adverse reactions | 310434 6CW7F3G59X |
| Gabapentin | GABAPENTIN | Bryant Ranch Prepack | 6a0a75ac-e121-477b-a9d1-d11f588afc9d | 2026-07-14 | Warnings, Adverse reactions | 6CW7F3G59X |
| Gabapentin | GABAPENTIN | Bryant Ranch Prepack | b6db5ce9-bd4b-420d-88a7-df9d46144c81 | 2026-07-10 | Warnings, Adverse reactions | ANDA203244 310434 6CW7F3G59X |
| Bombee Honey Daily Glow Shield Sunscreen | HOMOSALATE, OCTISALATE, OCTOCRYLENE, TITANIUM DIOXIDE | ABT ASIA Inc. | 56112dff-b091-7a56-e063-6294a90a77d3 | 2026-07-08 | Warnings | 15FIX9V2JP |
| Gabapentin | GABAPENTIN | PD-Rx Pharmaceuticals, Inc. | 9b175f8d-7667-4bfe-8bb5-fd7441eed456 | 2026-07-08 | Warnings, Adverse reactions | 310434 6CW7F3G59X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.