Penicillamine
- Product NDC
- 60505-4696
- 11-digit product format
- 605054696
- Labeler code
- 60505
- Product ID
- 60505-4696_8eefb301-f1c7-c392-1c6f-9a069ea34340
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Penicillamine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Apotex Corp.
- Application
- ANDA213310
- Marketing category
- ANDA
- Marketing start
- 2020-06-26
- Marketing end
- 0000-00-00
- Substance
- PENICILLAMINE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Antirheumatic Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- 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 |
|---|
| 60505-4696 | PENICILLAMINE (PENICILLAMINE) CAPSULE [APOTEX CORP.] | 4 | Legacy NDC | 20240423_4afb20ee-eb3f-1937-ffa4-5d3228e82688.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 60505-4696-1 | 60505469601 | 100 CAPSULE in 1 BOTTLE (60505-4696-1) | 100 capsule | 2020-06-26 | 0000-00-00 | No | No | Current |