NDC 16729-216-01 - SERTRALINE 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
- 16729-216
- Requested NDC
- 16729-216-01
- Package NDCs from labels
- 16729-216-10, 16729-216-15, 16729-216-01, 16729-216-16, 16729-216-43
- Manufacturer
- PD-Rx Pharmaceuticals, Inc.
- Effective date
- 2026-05-21
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| SERTRALINE HYDROCHLORIDE - PD-Rx Pharmaceuticals, Inc. | PD-Rx Pharmaceuticals, Inc. | 2026-05-21 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - Accord Healthcare, Inc. | Intas Pharmaceuticals Ltd | Accord Healthcare, Inc. | Intas Pharmaceuticals Ltd | 2025-12-17 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - QPharma, Inc. | Northwind Health Company, LLC | QPharma, Inc. | Northwind Health Company, LLC | 2025-12-15 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - Quality Care Products, LLC | Quality Care Products, LLC | 2024-12-18 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - REMEDYREPACK INC. | REMEDYREPACK INC. | 2024-09-24 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - Preferred Pharmaceuticals Inc. | Preferred Pharmaceuticals Inc. | 2024-08-07 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - Bryant Ranch Prepack | Bryant Ranch Prepack | 2024-04-03 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - RPK Pharmaceuticals, Inc. | RPK Pharmaceuticals, Inc. | 2023-08-18 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - RPK Pharmaceuticals, Inc. | RPK Pharmaceuticals, Inc. | 2023-08-18 | HUMAN PRESCRIPTION DRUG LABEL |
| Sertraline Hydrochloride - Direct Rx | Direct Rx | 2023-01-12 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - St. Mary's Medical Park Pharmacy | St. Mary's Medical Park Pharmacy | 2022-12-20 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - A-S Medication Solutions | A-S Medication Solutions | 2022-04-13 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - NuCare Pharmaceuticals,Inc. | NuCare Pharmaceuticals,Inc. | 2021-08-06 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - Unit Dose Services | Unit Dose Services | 2021-05-20 | HUMAN PRESCRIPTION DRUG LABEL |
| Sertraline Hydrochloride Tablets USP | NuCare Pharmaceuticals, Inc. | 2021-02-12 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - Denton Pharma, Inc. DBA Northwind Pharmaceuticals | Denton Pharma, Inc. DBA Northwind Pharmaceuticals | 2021-01-25 | HUMAN PRESCRIPTION DRUG LABEL |
| Sertraline Hydrochloride - Direct_Rx | Direct_Rx | 2021-01-07 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - Proficient Rx LP | Proficient Rx LP | 2019-11-01 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - Preferred Pharmaceuticals Inc. | Preferred Pharmaceuticals Inc. | 2019-04-26 | HUMAN PRESCRIPTION DRUG LABEL |
| SERTRALINE HYDROCHLORIDE - DIRECT RX | DIRECT RX | 2018-03-14 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 16729-216-01 | SERTRALINE HYDROCHLORIDE | 100 in 1 BOTTLE | TABLET, FILM COATED | 100 | 19 | |
| 16729-216-10 | SERTRALINE HYDROCHLORIDE | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | 19 | |
| 16729-216-15 | SERTRALINE HYDROCHLORIDE | 90 in 1 BOTTLE | TABLET, FILM COATED | 90 | 19 | |
| 16729-216-16 | SERTRALINE HYDROCHLORIDE | 500 in 1 BOTTLE | TABLET, FILM COATED | 500 | 19 | |
| 16729-216-43 | SERTRALINE HYDROCHLORIDE | 100 in 1 BOX, UNIT-DOSE | TABLET, FILM COATED | 100 | 19 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 16729-216-15 | EA - Each | 16729-216 | 244cfc50-a442-4123-bebc-3fe1dd4c1f78 | 1 | 2017-03-06 |
| 16729-216-16 | EA - Each | 16729-216 | 03832b5b-daa3-4a2f-90be-0c1e4075fed3 | 1 | 2017-03-06 |
DailyMed Socrata Ingredients#
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 |
|---|---|---|---|---|---|---|
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | HAMBLIN DERMATOLOGY | 5942e64c-416e-7525-e063-6394a90a2839 | 2026-08-17 | Warnings | 15FIX9V2JP |
| Protect Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | Opal Day Spa | 5943413a-48e1-0bdf-e063-6294a90a2fff | 2026-08-17 | Warnings | 15FIX9V2JP |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | MedSpa By Beauty Bar LLC | 5943ba3d-688e-9e9c-e063-6294a90afa9a | 2026-08-17 | Warnings | 15FIX9V2JP |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | CORBY, JR., TERRY L. | 594443fd-8e27-4ec6-e063-6294a90a3ff0 | 2026-08-17 | Warnings | 15FIX9V2JP |
| Leader Dry Eye Relief Eye Drops | GLYCERIN, HYPROMELLOSE, POLYETHYLENE GLYCOL 400 | CARDINAL HEALTH 110, LLC. DBA LEADER | 2ded4bda-b3c3-4521-8701-5c8446fd148b | 2026-08-17 | Warnings | B697894SGQ |
| Stay Ageless Tinted Mineral Sunscreen | BROAD SPECTRUM SPF30 | DR. SAMRAO'S OFFICE | 58b2ca35-11ed-d848-e063-6294a90a5b37 | 2026-08-11 | Warnings | 15FIX9V2JP |
| SYSTANE HYDRATION PF PRESERVATIVE FREE | POLYETHYLENE GLYCOL 400 AND PROPYLENE GLYCOL | Alcon Laboratories, Inc. | 8936f66f-10fe-44ab-a26e-dd8b05dfa997 | 2026-08-10 | Warnings | B697894SGQ |
| Journee Firm Riche Broad Spectrum Sunscreen SPF 30 | TITANIUM DIOXIDE AND ZINC OXIDE | Merz North America, Inc. | d4d4bfcf-3674-4847-8ad8-1716a8e821ae | 2026-08-10 | Warnings | 15FIX9V2JP |
| Sertraline Hydrochloride | SERTRALINE HYDROCHLORIDE | PD-Rx Pharmaceuticals, Inc. | adfcc867-1b6e-4698-94b6-2b4190c4ba3d | 2026-08-07 | Boxed warning, Warnings, Adverse reactions | 312941 UTI8907Y6X |
| Sertraline Hydrochloride | SERTRALINE HYDROCHLORIDE | PD-Rx Pharmaceuticals, Inc. | 52c88667-c67e-4d42-b319-afb354713b1e | 2026-08-07 | Boxed warning, Warnings, Adverse reactions | 312938 UTI8907Y6X |
| VEIRFOO Brightening Hydrating Antiwrinkle Sunscreen | TITANIUM DIOXIDE, OCTINOXATE | LCM TECHNOLOGY Co., Ltd | 4cbbf8aa-8910-b7e7-e063-6294a90a4f07 | 2026-08-07 | Warnings | 15FIX9V2JP |
| EltaMD UV Restore | TITANIUM DIOXIDE, ZINC OXIDE SUNSCREEN | CP Skin Health Group, Inc | 37fee381-ce6b-4949-9a4a-778aa839fb84 | 2026-08-06 | Warnings | 15FIX9V2JP |
| Leader Lubricant Eye Drops 30ct | POLYETHYLENE GLYCOL 400, PROPYLENE GLYCOL | CARDINAL HEALTH 110, LLC. DBA LEADER | 8df69f2c-40c4-245c-e053-2a95a90a5406 | 2026-08-05 | Warnings | B697894SGQ |
| Luxe Gloss Hydrating Lip Gloss SPF 35-NAKED HONEY | OCTOCRYLENE 8%, OCTISALATE 5%, TITANIUM DIOXIDE 6%, ZINC OXIDE 8% | Lale Cosmetics LLC | 581fb0cd-c55d-d562-e063-6394a90a7f11 | 2026-08-03 | Warnings | 15FIX9V2JP |
| EltaMD UV Active | ZINC OXIDE AND TITANIUM DIOXIDE SUNSCREEN | CP Skin Health Group, Inc | 39d16479-d491-4c19-aa11-674461687c7b | 2026-08-03 | Warnings | 15FIX9V2JP |
| Sertraline Hydrochloride | SERTRALINE HYDROCHLORIDE | Proficient Rx LP | 9dacf5b7-1a23-4767-a074-11f26623e48b | 2026-08-01 | Boxed warning, Warnings, Adverse reactions | 312938 UTI8907Y6X |
| Continuous Correction Cream | TITANIUM DIOXIDE | Baxter of California, LLC | 1cbcc648-f2e1-af60-e063-6294a90ad4bb | 2026-07-31 | Warnings | 15FIX9V2JP |
| Cover Creme | TITANIUM DIOXIDE | Baxter of California | 31f5e8c4-523f-4596-e063-6294a90a6a12 | 2026-07-31 | Warnings | 15FIX9V2JP |
| Sertraline Hydrochloride | SERTRALINE HYDROCHLORIDE | REMEDYREPACK INC. | 91e24d17-ff0a-449c-9472-b9df74c98456 | 2026-07-29 | Boxed warning, Warnings, Adverse reactions | 312941 UTI8907Y6X |
| Sertraline Hydrochloride | SERTRALINE HYDROCHLORIDE | REMEDYREPACK INC. | a2f333af-d37b-4705-ab7a-d363e3186e6e | 2026-07-24 | Boxed warning, Warnings, Adverse reactions | 312938 UTI8907Y6X |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.