Penicillamine
- Product NDC
- 43975-309
- 11-digit product format
- 439750309
- Labeler code
- 43975
- Product ID
- 43975-309_637901c4-0796-478b-8bbc-5860f0804f6b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Penicillamine
- Dosage form
- CAPSULE
- Route
- ORAL
- Labeler
- ANI Pharmaceuticals, Inc.
- Application
- ANDA209921
- Marketing category
- ANDA
- Marketing start
- 2019-05-07
- Marketing end
- 2022-06-30
- Substance
- PENICILLAMINE
- Active strength
- 250 mg/1
- Pharmacologic classes
- Antirheumatic Agent [EPC]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43975-309-10 | 43975030910 | 100 CAPSULE in 1 BOTTLE (43975-309-10) | 100 capsule | 2019-05-07 | 2022-06-30 | No | No | Current |