Phendimetrazine Tartrate
- Product NDC
- 63629-7266
- Requested package NDC
- 63629-7266-7
- 11-digit product format
- 636297266
- Labeler code
- 63629
- Product ID
- 63629-7266_2931767b-22b5-4d1d-9f57-00b49adb8995
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Phendimetrazine Tartrate
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA085588
- Marketing category
- ANDA
- Marketing start
- 1977-08-19
- Marketing end
- 0000-00-00
- Substance
- PHENDIMETRAZINE TARTRATE
- Active strength
- 35 mg/1
- Pharmacologic classes
- Appetite Suppression [PE],Increased Sympathetic Activity [PE],Sympathomimetic Amine Anorectic [EPC]
- DEA schedule
- CIII
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded package | package | 63629-7266 | 63629-7266-7 | D | Discontinued by firm | 2026-07-31 |
Orange Book products#
| Application-product | Trade name | Ingredient | Strength | Dosage form / route | TE codes | RLD / RS | Approval date |
|---|---|---|---|---|---|---|---|
| A085588-001 | PHENDIMETRAZINE TARTRATE | PHENDIMETRAZINE TARTRATE | 35MG | TABLET / ORAL | AA | Approved before 1982 |
Therapeutic equivalence codes#
| Application-product | TE code |
|---|---|
| A085588-001 | AA |
Observed Orange Book product history#
Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
| Captured | Edition | Application-product | Trade name | Strength | Dosage form / route | Product TE source text | RLD / RS | Approval date | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|
| 2026-08-01 22:54:32 | 2026-06 | A085588-001 | PHENDIMETRAZINE TARTRATE | 35MG | TABLET / ORAL | AA | Approved before 1982 | a50c72e98297… |
Observed Orange Book normalized TE history#
| Captured | Edition | Application-product | TE code | Order | Source SHA-256 |
|---|---|---|---|---|---|
| 2026-08-01 22:54:32 | 2026-06 | A085588-001 | AA | 1 | a50c72e98297… |
openFDA label cross-check#
Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| PHENDIMETRAZINE TARTRATE | PHENDIMETRAZINE TARTRATE | Bryant Ranch Prepack | 75f6c4bc-ed72-498a-822c-ecc2a13df958 | 2026-04-01 | Warnings, Adverse reactions | 085588 ANDA085588 |
| PHENDIMETRAZINE TARTRATE | PHENDIMETRAZINE TARTRATE | Virtus Pharmaceuticals, LLC | cc9a0cd2-6fb9-47ab-8e39-146d2fa361c2 | 2025-12-19 | Warnings, Adverse reactions | 085588 ANDA085588 |
| PHENDIMETRAZINE TARTRATE | PHENDIMETRAZINE TARTRATE | Bryant Ranch Prepack | 137e5fcd-9536-4fb9-9885-5dfd1127c35a | 2025-01-30 | Warnings, Adverse reactions | 085588 ANDA085588 |
FDA-Initiated Inactive NDC Indexing#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 63629-7266-1 | EA - Each | 63629-7266 | 49811e41-3600-4a4c-bd4e-ccc066166d6f | 1 | 2019-08-06 |
| 63629-7266-2 | EA - Each | 63629-7266 | 710f10de-c923-4059-9bcb-80200e4ce6b4 | 1 | 2019-08-06 |
| 63629-7266-3 | EA - Each | 63629-7266 | f65189c2-a576-4203-b4fd-53171781c4ca | 1 | 2019-08-06 |
| 63629-7266-4 | EA - Each | 63629-7266 | 5b0bca51-5a5a-4a9c-aa92-84581960fbd1 | 1 | 2019-08-06 |
| 63629-7266-5 | EA - Each | 63629-7266 | 7651a98c-7099-4af0-928e-ef57f88565e6 | 1 | 2019-08-06 |
| 63629-7266-6 | EA - Each | 63629-7266 | a0b9aae3-7704-4863-90b5-ade584045dc5 | 1 | 2019-08-06 |
| 63629-7266-7 | EA - Each | 63629-7266 | a69049ba-255f-42e9-a7af-89c5b048ba8e | 1 | 2019-08-06 |
| 63629-7266-8 | EA - Each | 63629-7266 | b3c227aa-4441-4487-80c3-43a159f1e3ed | 1 | 2019-08-06 |
Packages#
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|---|---|---|---|---|---|---|---|
| 63629-7266-7 | 63629726607 | 42 TABLET in 1 BOTTLE (63629-7266-7) | 42 tablet | 2017-04-25 | 0000-00-00 | No | No | Current |