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United States · US · US:75907-094_c77198dd-fd98-ac84-9754-517e77c5c729
Methamphetamine Hydrochloride
Orange BookUNIISPLATC N06BA03
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerDr. Reddy's Laboratories Inc
CountryUS (United States)
ATC codeN06BA03
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc117590709401100 TABLET in 1 BOTTLE, PLASTIC (75907-094-01)
Annotations
UNII (FDA Substance ID)
997F43Z9CV
METHAMPHETAMINE HYDROCHLORIDE
RxCUI 82044
Orange Book
A091189
AA
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "997F43Z9CV",
"rxcui": "82044",
"inchikey": "TWXDDNPPQUTEOV-FVGYRXGTSA-N",
"display_name": "METHAMPHETAMINE HYDROCHLORIDE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "ORAL",
"spl_meta": {
"d0905e2c-a02f-ec4f-59a3-6f7ad0acbbf6": {
"match": "brand_token",
"title": "METHAMPHETAMINE HYDROCHLORIDE TABLET [DR. REDDY'S LABORATORIES INC]",
"spl_version": "2",
"published_date": "2025-12-12"
}
},
"productid": "75907-094_c77198dd-fd98-ac84-9754-517e77c5c729",
"productndc": "75907-094",
"dosage_form": "TABLET",
"orange_book": {
"appl_no": "091189",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AA",
"strength": "5MG",
"product_no": "001",
"approval_date": "Apr 21, 2010"
}
],
"appl_type": "A"
},
"dea_schedule": "CII",
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "METHAMPHETAMINE HYDROCHLORIDE",
"proprietary_name": "Methamphetamine Hydrochloride",
"active_ingred_unit": "mg/1",
"application_number": "ANDA091189",
"marketing_category": "ANDA",
"nonproprietary_name": "METHAMPHETAMINE HYDROCHLORIDE",
"start_marketing_date": "20251107",
"active_numerator_strength": "5"
}Related drugs
Other records sharing ATC code N06BA03.
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