penicillamine
- Product NDC
- 68682-020
- 11-digit product format
- 686820020
- Labeler code
- 68682
- Product ID
- 68682-020_d757682f-6e86-47d9-a2f0-fb914bbcfadf
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- penicillamine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- Oceanside Pharmaceuticals
- Application
- NDA019853
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 1970-12-04
- 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 |
|---|
| 68682-020 | PENICILLAMINE CAPSULE [OCEANSIDE PHARMACEUTICALS] | 9 | Legacy NDC | 20210112_4af8b0be-06ad-481f-9cff-61601da8fdd1.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68682-020-10 | 68682002010 | 100 CAPSULE in 1 BOTTLE (68682-020-10) | 100 capsule | 1970-12-04 | 0000-00-00 | No | No | Current |