NDC 71335-1908-01 - Memantine Hydrochloride
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
- 71335-1908
- Requested NDC
- 71335-1908-01
- Package NDCs from labels
- 71335-1908-3, 71335-1908-4, 71335-1908-1, 71335-1908-2, 71335-1908-01
- Manufacturer
- Bryant Ranch Prepack
- Effective date
- 2024-04-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Memantine Hydrochloride - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-04-05 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 71335-1908-1 | Memantine Hydrochloride | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 102 | |
| 71335-1908-2 | Memantine Hydrochloride | 60 in 1 BOTTLE | TABLET, FILM COATED | 60 | 102 | |
| 71335-1908-3 | Memantine Hydrochloride | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 102 | |
| 71335-1908-4 | Memantine Hydrochloride | 180 in 1 BOTTLE | TABLET, FILM COATED | 180 | 102 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71335-1908 | MEMANTINE HYDROCHLORIDE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 102 | Current NDC, Legacy NDC, 4 package rows | 20240509_2ac7d23c-5f9f-4ffc-ae01-d7099a8a7929.zip |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71335-1908-1 | EA - Each | 71335-1908 | 02ce7c89-1e51-4986-af2f-cb3b81b9519f | 1 | 2022-06-06 |
| 71335-1908-2 | EA - Each | 71335-1908 | 434bda10-980a-42a9-bb5e-1ba9a0ee3357 | 1 | 2022-06-06 |
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 |
|---|---|---|---|---|---|---|
| Teething | ARNICA MONTANA, TRIFOLIUM PRATENSE, CALCAREA CARBONICA, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CHAMOMILLA, KREOSOTUM, SILICEA | BioActive Nutritional, Inc. | f39c9feb-f567-43a2-a026-2a581aeeed9d | 2016-07-27 | Warnings | ETJ7Z6XBU4 |
| Meijer Kids Tear Free SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Meijer Distribution, Inc. | 7415511e-1ecf-4646-b64b-267fbf7d116b | 2016-06-02 | Warnings | 15FIX9V2JP |
| Meijer Baby Tear Free SPF 50 | TITANIUM DIOXIDE, ZINC OXIDE | Meijer Distributing Inc. | 2434de23-bcc9-4a83-9945-16fc3f2b8c61 | 2016-06-01 | Warnings | 15FIX9V2JP |
| TOTAL DEFENSE REPAIR BROAD SPECTRUM SPF 34 Sunscreen (Tinted) | OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE AND ZINC OXIDE | Allergan, Inc. | 6a996e03-907f-4e6a-b232-0892b86956b0 | 2015-08-21 | Warnings | 15FIX9V2JP |
| Renewal Firming Day Broad Spectrum SPF 30 | TITANIUM DIOXIDE, ZINC OXIDE | BURT'S BEES, INC. | 18ceb5d8-4b76-6a54-e054-00144ff88e88 | 2015-06-18 | Warnings | 15FIX9V2JP |
| TiZO2 | TITANIUM DIOXIDE, ZINC OXIDE | Fallien Cosmeceuticals, LTD. | 30468afc-9616-4765-b046-12e97a0a7827 | 2010-12-20 | Warnings | 15FIX9V2JP |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.