Generic drug
- Product NDC
- 72567-001
- 11-digit product format
- 725670001
- Labeler code
- 72567
- Product ID
- 72567-001_d5c2f786-6d63-b5b8-e053-2995a90a00f7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Celecoxib
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Simcere of America, Inc.
- Application
- ANDA213598
- Marketing category
- ANDA
- Marketing start
- 2020-11-01
- Marketing end
- 0000-00-00
- Substance
- CELECOXIB
- Active strength
- 200 mg/1
- Pharmacologic classes
- Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Product Concepts#
FDA-Initiated Inactive NDC Indexing#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72567-001-01 | Generic drug | 100 in 1 BOTTLE | CAPSULE | 100 | | 6 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72567-001 | GENERIC DRUG (CELECOXIB) CAPSULE [SIMCERE OF AMERICA, INC.] | 6 | Legacy NDC, 1 package rows | 20220118_985ddcce-9734-4079-b413-3022661831e4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72567-001-01 | 72567000101 | 100 CAPSULE in 1 BOTTLE (72567-001-01) | 100 capsule | 2020-11-01 | 0000-00-00 | No | No | Current |