Penicillamine
- Product NDC
- 62559-970
- 11-digit product format
- 625590970
- Labeler code
- 62559
- Product ID
- 62559-970_b7c0ae76-9769-488d-a087-1e355eb21b35
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Penicillamine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA209921
- Marketing category
- ANDA
- Marketing start
- 2021-07-01
- Marketing end
- 0000-00-00
- Substance
- PENICILLAMINE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Antirheumatic Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 62559-970 | PENICILLAMINE CAPSULE [ANI PHARMACEUTICALS, INC.] | 4 | Legacy NDC | 20241215_b9527635-8f7a-4a77-b39c-cdf678cff827.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 62559-970-01 | 62559097001 | 100 CAPSULE in 1 BOTTLE (62559-970-01) | 100 capsule | 2021-07-01 | 0000-00-00 | No | No | Current |