Diphenhydramine Hydrochloride
- Product NDC
- 71335-0435
- 11-digit product format
- 713350435
- Labeler code
- 71335
- Product ID
- 71335-0435_b5a7fa2e-d908-49b7-8441-72a692a02614
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Diphenhydramine Hydrochloride
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- part341
- Marketing category
- OTC MONOGRAPH FINAL
- Marketing start
- 2009-01-02
- Marketing end
- 0000-00-00
- Substance
- DIPHENHYDRAMINE HYDROCHLORIDE
- Active strength
- 25 mg/1
- Pharmacologic classes
- Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 71335-0435 | D | Discontinued by firm | 2026-10-12 | ||
| excluded package | package | 71335-0435 | 71335-0435-0 | D | Discontinued by firm | 2026-10-12 | |
| excluded package | package | 71335-0435 | 71335-0435-1 | D | Discontinued by firm | 2026-10-12 | |
| excluded package | package | 71335-0435 | 71335-0435-2 | D | Discontinued by firm | 2026-10-12 | |
| excluded package | package | 71335-0435 | 71335-0435-3 | D | Discontinued by firm | 2026-10-12 | |
| excluded package | package | 71335-0435 | 71335-0435-4 | D | Discontinued by firm | 2026-10-12 | |
| excluded package | package | 71335-0435 | 71335-0435-5 | D | Discontinued by firm | 2026-10-12 | |
| excluded package | package | 71335-0435 | 71335-0435-6 | D | Discontinued by firm | 2026-10-12 | |
| excluded package | package | 71335-0435 | 71335-0435-7 | D | Discontinued by firm | 2026-10-12 | |
| excluded package | package | 71335-0435 | 71335-0435-8 | D | Discontinued by firm | 2026-10-12 | |
| excluded package | package | 71335-0435 | 71335-0435-9 | D | Discontinued by firm | 2026-10-12 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Dataset | Scope | Package NDC |
|---|---|---|
| excluded product | product | |
| excluded package | package | 71335-0435-8 |
| excluded package | package | 71335-0435-0 |
| excluded package | package | 71335-0435-9 |
| excluded package | package | 71335-0435-7 |
| excluded package | package | 71335-0435-3 |
| excluded package | package | 71335-0435-2 |
| excluded package | package | 71335-0435-4 |
| excluded package | package | 71335-0435-1 |
| excluded package | package | 71335-0435-5 |
| excluded package | package | 71335-0435-6 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 71335-0435-0 | EA - Each | 71335-0435 | 57d36003-e431-4e06-a09a-e1cf8e082b4c | 1 | 2018-03-08 |
| 71335-0435-1 | EA - Each | 71335-0435 | fbf130ae-4b14-4b48-b538-96ea9de817a2 | 1 | 2018-03-08 |
| 71335-0435-2 | EA - Each | 71335-0435 | 32bcefcf-b855-4aad-b5a7-a0c5db5c0eea | 1 | 2018-03-08 |
| 71335-0435-3 | EA - Each | 71335-0435 | f954522d-42b5-4793-968f-31492090b2cb | 1 | 2018-03-08 |
| 71335-0435-4 | EA - Each | 71335-0435 | b8fb5b11-6ad6-460e-9cf3-89bbdcb36a07 | 1 | 2018-03-08 |
| 71335-0435-5 | EA - Each | 71335-0435 | f5170598-c1bf-4ec8-b427-d826e1bcc05a | 1 | 2018-03-08 |
| 71335-0435-6 | EA - Each | 71335-0435 | d024b8f4-18ee-47cf-bfd3-ba34b13da54d | 1 | 2018-03-08 |
| 71335-0435-7 | EA - Each | 71335-0435 | 09a98da9-ee4c-412d-a0e1-168fd1b5cdd6 | 1 | 2018-03-08 |
| 71335-0435-8 | EA - Each | 71335-0435 | b1b04fdb-a818-4a87-8bd1-8db93cc392d9 | 1 | 2018-03-08 |
| 71335-0435-9 | EA - Each | 71335-0435 | d043d9f5-36c4-4b94-a360-b464233cb169 | 1 | 2018-03-08 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 71335-0435 | DIPHENHYDRAMINE HYDROCHLORIDE CAPSULE [BRYANT RANCH PREPACK] | 9 | Legacy NDC | 20250221_b5a7fa2e-d908-49b7-8441-72a692a02614.zip |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 71335-0435-0 | 71335043500 | 100 CAPSULE in 1 BOTTLE (71335-0435-0) | 100 capsule | 2017-05-02 | 0000-00-00 | No | No | Current |
| 71335-0435-1 | 71335043501 | 30 CAPSULE in 1 BOTTLE (71335-0435-1) | 30 capsule | 2017-05-02 | 0000-00-00 | No | No | Current |
| 71335-0435-2 | 71335043502 | 20 CAPSULE in 1 BOTTLE (71335-0435-2) | 20 capsule | 2017-05-02 | 0000-00-00 | No | No | Current |
| 71335-0435-3 | 71335043503 | 42 CAPSULE in 1 BOTTLE (71335-0435-3) | 42 capsule | 2017-05-02 | 0000-00-00 | No | No | Current |
| 71335-0435-4 | 71335043504 | 24 CAPSULE in 1 BOTTLE (71335-0435-4) | 24 capsule | 2017-05-02 | 0000-00-00 | No | No | Current |
| 71335-0435-5 | 71335043505 | 15 CAPSULE in 1 BOTTLE (71335-0435-5) | 15 capsule | 2017-05-02 | 0000-00-00 | No | No | Current |
| 71335-0435-6 | 71335043506 | 60 CAPSULE in 1 BOTTLE (71335-0435-6) | 60 capsule | 2017-05-02 | 0000-00-00 | No | No | Current |
| 71335-0435-7 | 71335043507 | 10 CAPSULE in 1 BOTTLE (71335-0435-7) | 10 capsule | 2017-05-02 | 0000-00-00 | No | No | Current |
| 71335-0435-8 | 71335043508 | 6 CAPSULE in 1 BOTTLE (71335-0435-8) | 6 capsule | 2017-05-02 | 0000-00-00 | No | No | Current |
| 71335-0435-9 | 71335043509 | 90 CAPSULE in 1 BOTTLE (71335-0435-9) | 90 capsule | 2017-05-02 | 0000-00-00 | No | No | Current |