Belladonna and Opium
- Product NDC
- 73577-030
- 11-digit product format
- 735770030
- Labeler code
- 73577
- Product ID
- 73577-030_5820d813-646c-4d00-9763-0747e3200e8e
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- ATROPA BELLADONNA and OPIUM
- Dosage form
- SUPPOSITORY
- Route
- RECTAL
- Labeler
- Legacy Pharma Inc.
- Marketing category
- UNAPPROVED DRUG OTHER
- Marketing start
- 2020-04-29
- Marketing end
- 0000-00-00
- Substance
- ATROPA BELLADONNA; OPIUM
- Active strength
- 16 mg/1; mg/1
- DEA schedule
- CII
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- Current FDA listing
- Historical FDA.report record
NDC auxiliary status#
Explicit status records from FDA unfinished, excluded, and compounder auxiliary files. Absence of a row is not itself a regulatory status. Browse every current auxiliary row, including rows without a usable NDC. · Browse every captured source and parsed snapshot.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 73577-030 | D | Discontinued by firm | 2026-08-03 | ||
| excluded package | package | 73577-030 | 73577-030-12 | D | Discontinued by firm | 2026-08-03 |